Radicicol derivatives

ABSTRACT

Radioicol derivatives represented by the following formula (I) having tyrosine kinase inhibition activity or pharmacologically acceptable salts thereof:                    
     wherein R 1  and R 2  are the same or different, and each represents hydrogen, alkanoyl, alkenoyl, tert-butyldiphenylsilyl or tert-butyldimethylsilyl; R 3  represents Y—R 5  (wherein Y represents substituted or unsubstituted alkylene; and R 5  represents CONR 6 R 7  (wherein R 6  represents hydrogen, hydroxyl, substituted or unsubstituted lower alkyl, substituted or unsubstituted higher alkyl, and the like; R 7  represents hydroxyl, substituted lower alkyl, and the like), CO 2 R 12  (wherein R 12  represents substituted lower alkyl, substituted or unsubstituted higher alkyl, and the like), and the like) and the like; X represents halogen or is combined together with R 4  to represent a single bond; and R 4  is combined together with X to represent a single bond, or represents hydrogen, alkanoyl, and the like.

TECHNICAL FIELD

This application is a 371 of PCT/JP97/03874 filed on Oct. 24, 1997.

The present invention relates to novel radicicol derivatives orpharmacologically acceptable salts thereof which show tyrosine kinaseinhibition activity and have antitumor or immunosuppression effects.

BACKGROUND ART

It is known that microbial metabolite radicicol represented by thefollowing formula (B) has an antifungal effect and an anticancer effect[Nature, 171, 344 (1953); Neoplasma, 24, 21 (1977)], animmunosuppression effect (Japanese Published Unexamined PatentApplication No. 298764/94), or morphology normalization effect of ras ormos canceration cells [Oncogene, 11, 161 (1995)].

Furthermore, it is known that radicicol derivatives in which thephenolic hydroxyl group is modified with various acyl groups have anantitumor effect (Japanese Published Unexamined Patent Application No.226991/92). In addition, it is disclosed that radicicol derivatives inwhich the phenolic hydroxyl group is modified with an acyl group or analkyl group show an angiogenesis inhibition effect (Japanese PublishedUnexamined Patent Application No. 279279/94) or an interleukin 1production inhibition effect (Japanese Published Unexamined PatentApplication No. 40893/96). Recently, oxime derivatives of dienone of aradicicol derivative showing antitumor action and immunosuppressionaction have been published (WO 96/33989; published on Oct. 31, 1996),and antitumor radicicol derivatives represented by the following formula(B′) have also been published (Japanese Published Unexamined PatentApplication 202781/97: published on Aug. 5, 1997).

(In the formula, R^(1p) and R^(2p) represent a hydrogen atom or an acylgroup; and X^(P) represents a halogen atom, a hydroxyl group or a loweralkoxy group.)

Additionally, it is known that ansamycins antibiotics, geldanamycin,represented by formula (C) [The Journal of Antibiotics, 23, 442 (1970)]has tyrosine kinase inhibition activity and antitumor effects [forexample, Cancer Research, 52, 1721 (1992) and Cancer Research 54, 2724(1994)]. It is shown that these effects are expressed by the inhibitionof the activation of a tyrosine kinase, such as Src, ErbB-2, Lck or thelike, and a serine/threonine kinase Raf-1, through the formation of acomplex of geldanamycin with a molecular chaperone Hsp (heatshock/stress protein) 90 by binding to Hsp90 [for example, Proceedingsof the National Academy of Sciences of the U.S.A., 91, 8324 (1994) andThe Journal of Biological Chemistry, 270, 24585 (1995)]. Consequently,drugs capable of acting upon Hsp90 are also included in tyrosine kinaseinhibitors and useful not only as antitumor agents but also for theprevention and treatment of various diseases such as osteoporosis,immune diseases, and the like.

Tyrosine kinase is an enzyme which uses ATP as a phosphate donor andcatalyzes transfer of its γ-phosphate group to the hydroxyl group of aspecified tyrosine residue of a substrate protein, thereby taking animportant role in the control mechanism of intracellular signaltransduction. Various tyrosine kinase families are known. Tyrosinekinase activities, such as Src in colon cancer, ErbB-2 in breast cancerand gastric cancer, Ab1 in leukemia, and the like, increase. Disorderedincrease in the tyrosine kinase activity causes abnormal differentiationand proliferation of cells. Consequently, specific inhibitors oftyrosine kinase are useful in preventing and treating various diseases,including as antitumor agents.

Lck is a tyrosine kinase which is activated when T lymphocytes areactivated by antigen stimulation, and an inhibitor of this enzyme isuseful as an immunosuppressant. Also, it is known that Src relates tobone resorption in osteoclast, and an inhibitor of this tyrosine kinaseis useful as a bone resorption inhibitor for the treatment ofosteoporosis. Additionally, inhibitors of receptor type tyrosine kinasesof various growth factors, such as EGF-R (epidermal growth factorreceptor), FGF-R (fibroblast growth factor receptor), PDGF-R(platelet-derived growth factor receptor), and the like, are useful as asolid cancer growth inhibitor, an angiogenesis inhibitor, a vascularsmooth muscle growth inhibitor, and the like.

DISCLOSURE OF THE INVENTION

An object of the present invention is to provide novel radicicolderivatives or pharmacologically acceptable salts thereof which showtyrosine kinase inhibition activity and have antitumor orimmunosuppression effects.

The present invention can provide radicicol derivatives represented bythe following formula (I) or pharmacologically acceptable salts thereof:

wherein R¹ and R² are the same or different, and each representshydrogen, alkanoyl, alkenoyl, tert-butyldiphenylsilyl ortert-butyldimethylsilyl;

R³ represents:

Y—R⁵ (wherein Y represents substituted or unsubstituted alkylene; and R⁵represents CONR⁶R⁷ (wherein R⁶ represents hydrogen, hydroxyl,substituted or unsubstituted lower alkyl, substituted or unsubstitutedhigher alkyl, substituted or unsubstituted lower cycloalkyl, substitutedor unsubstituted alkenyl, substituted or unsubstituted lower alkoxy,substituted or unsubstituted aryl, a substituted or unsubstitutedheterocyclic group, or NR⁸R⁹ (wherein R⁸ and R⁹ are the same ordifferent, and each represents hydrogen, substituted or unsubstitutedlower alkyl, substituted or unsubstituted higher alkyl, substituted orunsubstituted lower cycloalkyl, substituted or unsubstituted aryl, asubstituted or unsubstituted heterocyclic group, substituted orunsubstituted alkanoyl, substituted or unsubstituted aroyl, carbonylbound to a substituted or unsubstituted heterocyclic ring, orsubstituted or unsubstituted arylcarbamoyl), or is combined togetherwith R⁷ and adjoining N to represent a substituted or unsubstitutedheterocyclic group; and R⁷ is combined together with R⁶ and adjoining Nto represent a substituted or unsubstituted heterocyclic group, orrepresents hydroxyl, substituted lower alkyl, substituted orunsubstituted higher alkyl, substituted or unsubstituted lowercycloalkyl, substituted or unsubstituted alkenyl, substituted orunsubstituted lower alkoxy, substituted or unsubstituted aryl, asubstituted or unsubstituted heterocyclic group, or NR¹⁰R¹¹ (wherein R¹⁰and R¹¹ have the same meaning as R⁸ or R⁹ defined above, respectively)>,CO₂R¹² (wherein R¹² represents substituted lower alkyl, substituted orunsubstituted higher alkyl, substituted or unsubstituted lowercycloalkyl, substituted or unsubstituted alkenyl, substituted orunsubstituted aryl, or a substituted or unsubstituted heterocyclicgroup), substituted or unsubstituted aryl, substituted or unsubstitutedpyridyl, substituted or unsubstituted pyridonyl, substituted orunsubstituted pyrrolidonyl, substituted or unsubstituted uracilyl,substituted or unsubstituted piperidyl, substituted or unsubstitutedpiperidino, substituted or unsubstituted pyrrolidinyl, substituted orunsubstituted morpholino, substituted or unsubstituted morpholinyl,substituted or unsubstituted piperzazinyl, substituted or unsubstitutedthiomorpholino, or substituted or unsubstituted dioxolanyl}.

COR¹³ (wherein R¹³ represents hydrogen, substituted or unsubstitutedlower alkyl, substituted or unsubstituted higher alkyl, substituted orunsubstituted aryl, substituted or unsubstituted lower alkoxy, orNR¹⁴R¹⁵ (wherein R¹⁴ and R¹⁵ are the same or different, and eachrepresents hydrogen, substituted or unsubstituted lower alkyl,substituted or unsubstituted higher alkyl, substituted or unsubstitutedaryl, or substituted or unsubstituted pyridyl, or R¹⁴ and R¹⁵ arecombined together with adjoining N to represent a substituted orunsubstituted heterocyclic group)>, or

substituted or unsubstituted aryl;

X represents halogen, or is combined together with R⁴ to represent asingle bond; and

R⁴ is combined together with X to represent a single bond, or representshydrogen, alkanoyl, alkenoyl, or —SO—Z {wherein Z represents formula(A):

wherein R^(1A) and R^(2A) have the same meaning as R¹ and R² definedabove, respectively; X⁴ represents halogen; and W represents O orN—O—R^(3A) (wherein R^(3A) has the same meaning as R³ defined above)}.

Hereinafter, the compound represented by formula (I) will be calledcompound (I). Compounds of other formula numbers with also be called inthe same manner.

(1) Explanation of each group

In the definition of each group of compound (I), the term “lower” means1 to 8 carbon atoms, and the term “higher” means 9 to 30 carbon atoms,unless otherwise indicated.

Examples of the alkanoyl include straight or branched groups having 1 to30 carbon atoms, such as formyl, acetyl, propanoyl, isopropanoyl,butanoyl, caproyl, lauroyl, myristoyl, palmitoyl, stearoyl, and thelike. Examples of the alkenoyl include straight or branched groupshaving 3 to 30 carbon atoms, such as acryloyl, methacryloyl, crotonoyl,isocrotonoyl, palmitoleoyl, linoleoyl, linolenoyl, and the like.Examples of the alkyl moiety of the lower alkyl and the lower alkoxyinclude straight or branched groups, such as methyl, ethyl, propyl,isopropyl, butyl, isobutyl, sec-butyl, tert-butyl, pentyl, isopentyl,neopentyl, hexyl, heptyl, octyl, isooctyl, and the like, and one of thecarbon atoms thereof may be substituted with a silicon atom. Examples ofthe higher alkyl include straight or branched groups, such as decanyl,dodecyl, hexadecyl, and the like. Examples of the alkenyl includestraight or branched groups having 2 to 30 carbon atoms, such as vinyl,allyl, 1-propenyl, 2-butenyl, 1-pentenyl, 2-hexenyl, 1,3-pentadienyl,1,3-hexadienyl, dodecenyl, hexadecenyl, and the like. Examples of thelower cycloalkyl include groups having 3 to 8 carbon atoms, such ascyclopropyl, cyclobutyl, cyclopentyl, cyclohexyl, cyclooctyl, and thelike. Examples of the aryl include phenyl, naphthyl, and the like, andthe aryl moiety of aroyl and arylcarbamoyl has the same meaning.Examples of the heterocyclic group include alicyclic heterocyclicgroups, aromatic heterocyclic groups, and the like, such as pyridonyl,pyrrolidonyl, uracilyl, dioxolnyl, pyrrolyl, tetrazolyl, pyrrolidinyl,thienyl, morpholino, thiomorpholino, piperazinyl, pyrazolidinyl,piperidino, pyridyl, hompiperazinyl, pyrazolyl, pyrazinyl, indolyl,isoindolyl, furyl, piperidyl, quinolyl, phthalazinyl, imidazolidinyl,imidazolinyl, pyrimidinyl, and the like. The heterocylic group moiety inthe carbonyl bound to a heterocyclic ring has the same meaning asdefined above, and examples of the entire group containing carbonylinclude furoyl, thenoyl, nicotinoyl, isonicotinoyl, and the like.Examples of the nitrogen containing heterocyclic group formed by R⁶ andR⁷ with the adjoining N and the nitrogen containing heterocyclic groupformed by R¹⁴ and R¹⁵ with the adjoining N (said heterocyclic group mayfurther contain O, S or other N) include pyrrolidyl, morpholino,thiomorpholino, piperazinyl, pyrazolidinyl, pyrazolinyl, piperidino,homopiperazinyl, indolinyl, isoindolinyl, perhydroazepinyl,perhydroazocinyl, indolyl, isoindolyl, and the like. Examples of thealkylene include those groups in which one hydrogen atom is removed fromthe group of alkyl moiety of the above lower alkyl or higher alkyl.Examples of the halogen include fluorine, chlorine, bromine and iodineatoms.

(2) Explanation of substituent in each group

Examples of the substituent in the substituted lower alkyl, thesubstituted higher alkyl, the substituted alkenyl, the substituted loweralkoxy and the substituted alkanoyl include 1 to 3 substituents, whichare the same or different, such as hydroxyl, lower cycloalkyl, lowercycloalkenyl, lower alkoxy, lower alkanoyloxy, azido, amino, mono- ordi-lower alkylamino, mono- or di-lower alkanoylamino, loweralkoxycarbonylamino, lower alkenyloxycarbonylamino, halogen, loweralkanoyl, substituted or unsubstituted aryl, a substituted orunsubstituted heterocyclic group, cyclic imido (a group formed byremoving hydrogen bound to an imido N atom), CONR¹⁶R¹⁷ (wherein R¹⁶ andR¹⁷ are the same or different, and each represents hydrogen, hydroxyl,lower alkyl, lower cycloalkyl, higher alkyl, alkenyl, lower alkoxy,aryl, a heterocyclic group, or NR¹⁸R¹⁹ (wherein R¹⁸ and R¹⁹ are the sameor different, and each represents hydrogen, lower alkyl, lowercycloalkyl, aryl, a heterocyclic group, lower alkanoyl, aroyl, carbonylbound to a heterocyclic ring, or arylcarbamoyl)>, CO₂R²⁰ (wherein R²⁰represents hydrogen, lower alkyl, higher alkyl, lower cycloalkyl,alkenyl, substituted or unsubstituted aryl, or a substituted orunsubstituted heterocyclic group), or —(OCH₂CH₂)_(n)OCH₃ (wherein n isan integer of 1 to 10).

Examples of the substituent in the substituted alkylene include 1 to 3substituents, which are the same or different, such as hydroxyl, loweralkoxy, lower alkanoyloxy, azido, amino, mono- or di-lower alkylamino,mono- or di-lower alkanoylamino, lower alkoxycarbonylamino, loweralkenyloxycarbonylamino, halogen, lower alkanoyl, substituted orunsubstituted aryl, substituted or unsubstituted pyridyl, substituted orunsubstituted pyridonyl, substituted or unsubstituted pyrrolidonyl,substituted or unsubstituted uracilyl, substituted or unsubstitutedpiperidyl, substituted or unsubstituted piperidino, substituted orunsubstituted pyrrolidinyl, substituted or unsubstituted morpholino,substituted or unsubstituted morpholinyl, substituted or unsubstitutedpiperazinyl, substituted or unsubstituted thiomorpholino, substituted orunsubstituted dioxolanyl, cyclic imido (a group formed by removinghydrogen bound to an imido N atom), CONR¹⁶R¹⁷ (wherein R¹⁶ and R¹⁷ havethe same meaning as defined above), or CO₂R²⁰ (wherein R²⁰ has the samemeaning as defined above).

Examples of the substituent in the substituted lower cycloalkyl, thesubstituted aryl, the substituted heterocyclic group, the substitutedaroyl, the carbonyl bound to a substituted heterocyclic ring, thesubstituted arylcarbamoyl, the substituted pyrrolidonyl, the substituteduracilyl, the substituted piperidyl, the substituted piperidino, thesubstituted pyrrolidinyl, the substituted morpholino, the substitutedmorpholinyl, the substituted piperazino, the substituted piperazinyl,the substituted thiomorpholino, the substituted dioxolanyl and thesubstituted nitrogen containing heterocyclic group formed with theadjoining N include 1 to 3 substituents, which are the same ordifferent, such as hydroxyl, lower alkyl, lower alkyl substituted with aheterocyclic ring (said heterocyclic ring may be substituted with loweralkyl), higher alkyl, alkenyl, lower cycloalkyl, lower cycloalkenyl,lower alkoxy, lower alkoxy-lower alkoxy, lower alkanoyloxy, azido,amino, mono- or di-lower alkylamino, mono- or di-lower alkanoylamino,lower alkoxycarbonylamino, lower alkenyloxycarbonylamino, halogen, loweralkanoyl, aryl, a heterocyclic group, cyclic imido (a group formed byremoving hydrogen bound to an imido N atom), CONR¹⁶R¹⁷ (wherein R¹⁶ andR¹⁷ have the same meaning as defined above), CO₂R²⁰ (wherein R²⁰ has thesame meaning as defined above), or SO₂NR²¹R²² (wherein R²¹ and R²² arethe same or different, and each represents hydrogen or lower alkyl). Thelower alkyl, the higher alkyl, the alkenyl, the lower cycloalkyl, thelower alkoxy, the halogen, the aryl, the aroyl, the arylcarbamoyl, theheterocyclic group, and the carbonyl bound to a heterocyclic ring usedherein have the same meaning as defined above. The lower alkyl moietiesof the mono- or di-lower alkylamino, the lower alkoxycarbonyl, the loweralkoxycarbonylamino, and the lower alkoxy-lower alkoxy have the samemeaning as defined above. The lower alkenyl moiety of the loweralkenyloxycarbonylamino means the above alkenyl group having 2 to 8carbon atoms, such as vinyl, allyl, 1-propenyl, 2-butenyl, 1-pentenyl,2-hexenyl, 1,3-pentadienyl, 1,3-hexadienyl, and the like. Examples ofthe lower cycloalkenyl include those having 4 to 8 carbon atoms, such as2-cyclopentenyl, 2-cyclohexenyl, 1,3-cyclopentadienyl, and the like.Examples of the lower alkanoyl moiety of the lower alkanoyl, the loweralkanoyloxy and the mono- or di-lower alkanoylamino include straight orbranched groups having 1 to 8 carbon atoms, such as formyl, acetyl,propanoyl, isopropanoyl, butanoyl, caproyl, and the like. Examples ofthe cyclic imido include phthalimido, succinimido, glutarimido, and thelike.

As compound (I), compounds in which X is a halogen are preferred, andcompounds in which X is combined together with R⁴ to represent a singlebond are also preferred. Among the compounds in which X is combinedtogether with R⁴ to represent a single bond, compounds in which R¹ andR² are hydrogen are preferred. Among these, compounds in which R³(wherein R³ has the same meaning as defined above) is Y-R⁵ (wherein R⁵has the same meaning as defined above) are more preferred. Among thecompounds in which X is combined together with R⁴ to represent a singlebond, compounds in which R¹ and R² are hydrogen, R³ is Y-R⁵ (wherein R⁵has the same meaning as defined above) and R⁵ is substituted orunsubstituted aryl, and the like, are most preferred, and among these,compounds in which R⁵ is pyrrolidonyl are particularly preferred.

The pharmacologically acceptable salts of compound (I) include acidaddition salts, metal salts, ammonium salts, organic amine additionsalts, amino acid addition salts, and the like. Examples of the acidaddition salts include inorganic acid salts (for example, hydrochloride,hydrobromide, sulfate, phosphate, and the like), and organic acid salts(for example, formate, acetate, oxalate, benzoate, methanesulfonate,p-toluenesulfonate, maleate, fumarate, tartrate, citrate, succinate,lactate, and the like). Examples of the metal salts include alkali metalsalts (for example, lithium salt, sodium salt, potassium salt, and thelike), alkaline earth metal salts (for example, magnesium salt, calciumsalt, and the like), aluminum salts, zinc salts, and the like. Examplesof the ammonium salts include salts with ammonium, tetramethylammonium,and the like. Examples of the organic amine addition salts includeaddition salts with morpholine, piperidine, and the like. Examples ofthe amino acid addition salts include addition salts with glycine,phenylalanine, aspartic acid, glutamic acid, lysine, and the like.

The compound of the present invention is generally prepare usingradicicol as a starting material. Compound (I) may contain variousstereoisomers, geometric isomers, tautomeric isomers, and the like. Allof possible isomers and their mixtures are includes in the presentinvention, and the mixing ratio is not particularly limited.

A production method of compound (I) is described below.

The production method of compound (I) mainly comprises oxime formation(production method 1), acylation/carbamoylation/alkoxycarbonylation(production method 2), alkylation (production method 3),amidation/esterification (production method 4), desilylation (productionmethod 5), halohydrination (production method 6), silylation (productionmethod 7), and acylation (production method 8), and each compound ofinterest is produced by combining these reaction steps depending on theobject.

In the production method shown below, when a defined group changes underconditions of the employed method or is not fit for carrying out themethod, the compound of interest can be prepared using anintroduction-elimination method of protecting groups usually used insynthetic organic chemistry [for example, see Protective Groups inOrganic Synthesis, T. W. Greene, John Wiley & Sons Inc. (1981)]. Asoccasion demands, the sequence of reaction steps, such as introductionof substituent groups and the like, may be changed.

Production method 1

Compound (Ia) can be prepared according to following reaction step, byoxime formation of the dienone carbonyl of radicicol, compound (D) whichis prepared from radicicol by a known method (Japanese PublishedUnexamined Patent Application No. 226991/92) or compound (E) which isprepared from radicicol or a radicicol derivative in which one of thephenolic hydroxyl groups is substituted with alkanoyl or alkenoyl inaccordance with a known method [for example, Journal of the AmericanChemical Society, 94, 6190 (1972)].

[In the above reaction formula, R^(1a) and R^(2a) represent groups inwhich tert-butyldimethylsilyl and tert-butyldiphenylsilyl are removedfrom R¹ and R² described above; R^(1b) and R^(2b) represent groups inwhich at least one of R¹ and R² described above is substituted withtert-butyldimethylsilyl or tert-butyldiphenylsilyl; R^(3a) is a group inwhich COR¹³ (wherein R¹³ has the same meaning as described above) isremoved from R³ described above; and R¹ and R² have the same meaning asdefined above.]

Step 1

Compound (Ia) can be prepared by allowing compound (D) or compound (E)to react with compound (II) represented by the following formulaH₂N—O—R^(3a) (II) (wherein R^(3a) has the same meaning as defined above)or an acid addition salt thereof.

Examples of the reaction solvent include pyridine, chloroform,dichloromethane, ethyl acetate, ether, tetrahydrofuran (THF),dimethylformamide (DMF), acetonitrile, and the like, which may be usedeither alone or as a mixture thereof, and pyridine is preferred.Examples of the acid including hydrochloric acid, acetic acid,trifluoroacetic acid, sulfuric acid, p-toluenesulfonic acid,camphorsulfonic acid, and the like, and they are preferably used in anamount of 0.1 to 10 equivalents based on compound (D) or (E). When anacid addition salt of compound (II) is used, the reaction can be carriedout in the presence of a base, for example, amines (e.g., pyridine,triethylamine, diisopropylethylamine, N,N-dimethylaniline,N,N-diethylaniline, or the like) or alkali metal carbonate orbicarbonate (e.g., sodium carbonate, potassium carbonate, or the like),in an amount of 1 equivalent or more based on the acid addition salt ofcompound (II), preferably using pyridine which also serves as thesolvent. The compound (II) or an acid addition salt thereof is used inan amount of 1 equivalent or more, preferably 1 to 5 equivalents, basedon compound (D) or (E). The reaction is carried out at a temperature of−20 to 100° C., preferably 20 to 60° C., and the reaction completesafter 1 to 80 hours.

Production method 2

Compound (Ib) can be prepared by the steps in which compound (F) isconverted into oxime compound (G), and then the resulting hydroxyl groupis subjected to acylation, carbamoylation or alkoxycarbonylation.

[In the above reaction formula, R^(1c) and R^(2c) are the same ordifferent, and each represents alkanoyl, alkenoyl,tert-butyldimethylsilyl or tert-butyldiphenylsilyl, and R^(3b)represents COR¹³ (wherein R¹³ has the same meaning as defined above).]

Step 2-1

Compound (G) can be prepared by allowing compound (F) to react withhydroxylamine or an acid addition salt thereof according to method ofthe above step 1.

Step 2-2

Compound (Ib) can be prepared by allowing compound (G) to react withcompound (III) represented by the following formula R¹³COCl (III)(wherein R³ has the same meaning as defined above), or with compound(IV) represented by the following formula R²³NCO (IV) (wherein R²³represents substituted or unsubstituted lower alkyl, substituted orunsubstituted higher alkyl, substituted or unsubstituted aryl, orsubstituted or unsubstituted pyridyl), in the presence of a base.

As the reaction solvent, dichloromethane, ether, THF, DMF, and the like,may be used alone or as a mixture thereof. As the base, amines (forexample, pyridine, triethylamine, diisopropylethylamine, or the like)are used in an amount of 0.1 equivalent or more, preferably 1 to 10equivalents, based on compound (III) or (IV). Compound (III) or (IV) isused in an amount of 1 equivalent or more, preferably 1 to 5equivalents, based on compound (G). The reaction is carried out at atemperature of −80 to 100° C., preferably −80 to 0° C., when compound(III) is used, or at a temperature of 0 to 80° C. when compound (IV) isused, and each reaction completes after 10 minutes to 48 hours.

Production method 3

Compound (Ic) can be prepared by a step in which the hydroxyl group ofthe above compound (G) is alkylated.

[In the above reaction formula, R^(3c) represents Y-R⁵ (wherein Y and R⁵have the same meaning as defined above), and R^(1c) and R^(2c) have thesame meaning as defined above.]

Step 3

Compound (Ic) can be prepared by allowing compound (G) to react withcompound (V) represented by the following formula HOR²⁴ (V) (wherein R²⁴has the same meaning as R^(3c) defined above) in the presence of acondensing agent.

As the reaction solvent, toluene, THF, dichloromethane, and the like,are used alone or as a mixture thereof. As the condensing agent,trivalent phosphorous compounds (for example, triphenylphosphine,tributylphosphine, or the like) and azo compounds (for example, diethylazodicarboxylate (DEAD), 1,1-(azodicarbonyl)dipiperidine, and the like)are used as a mixture thereof. Each of compound (V) and the condensingagent is used in an amount of 1 equivalent or more, preferably 1 to 5equivalents, based on compound (G). The reaction is carried out at atemperature of −20 to 80° C., preferably 0 to 30° C., and the reactioncompletes after 5 minutes to 48 hours.

Production method 4

Compound (Id) can be prepared by step in which compound (H) is convertedinto oxime compound (J) in which a carboxyl group is introduced, andthen the carboxyl group is subjected to amidation or esterification.

{In the above reaction formula, R^(3d) represents Y-R^(5a) [whereinR^(5a) represents CONR⁶R⁷ (wherein R⁶ and R⁷ have the same meaning asdefined above) or CO₂R¹² (wherein R¹² has the same meaning as definedabove), and Y has the same meaning as defined above], and Y, R¹ and R²have the same meaning as defined above.}

Step 4-1

Compound (J) can be prepared by allowing compound (H) to react withcompound (VI) represented by the following formula H₂N—O—Y—CO₂H (VI)(wherein Y has the same meaning as defined above) or an acid additionsalt thereof according to the method of the above step 1.

Step 4-2

Compound (Id) can be prepared by allowing compound (J) to react withcompound (VII) represented by the following formula HNR⁶R⁷ (VII)(wherein R⁶ and R⁷ have the same meaning as defined above) or an acidaddition salt thereof, or with a compound (VIII) represented by thefollowing formula HOR¹² (VIII) (wherein R¹² has the same meaning asdefined above), in the presence of a condensing agent.

As the condensing agent, 1-(3-dimethylaminopropyl)-3-ethylcarbodiimidehydrochloride (EDCI), N,N′-dicyclohexylcarbodiimide (DCC),1,1′-carbonyldiimidazole, or the like, is used. Additionally, thereaction can be accelerated by adding an additive agent, such asN-hydroxysucciniimide (HONSu), 4-(dimethylamino)pyridine (DMAP),1-hydroxybenzotriazole hydrate (HOBt), or the like, in an amount of 0.1to 5 equivalents based on compound (J). As the reaction solvent,dichloromethane, ether, THF, DMF, and the like, may be used alone or asa mixture thereof. When an acid addition salt of compound (VII) is used,the reaction can be carried out in the presence of a base, such asamines (for example, pyridine, triethylamine, diisopropylethylamine, orthe like), preferably triethylamine, in an amount of 1 equivalent ormore, preferably 1 to 10 equivalents, based on the acid addition salt ofcompound (VII). Each of compound (VII) or an acid addition salt thereofor compound (VIII) and the condensing agent is used in an amount of 1equivalent or more, preferably 1 to 5 equivalents, based on compound(J). The reaction is carried out at a temperature of −20 to 80° C.preferably 0 to 40° C., and each reaction completes after 10 minutes to48 hours.

Production method 5

Compound (If) can be prepared by carrying out desilylation of compound(Ie) which is a derivative compound of (I) in which at least one of R¹and R² is substituted with tert-butyldimethylsilyl ortert-butyldiphenylsilyl.

(In the above reaction formula, R^(1b), R^(2b) and R³ have the samemeaning as defined above, and R^(1d) and R^(2d) are groups in which atleast one of tert-butyldimethylsilyl or tert-butyldiphenylsilyl of theabove R^(1b) and R^(2b) is substituted with hydrogen.)

Step 5

Compound (If) can be prepared by allowing compound (Ie) to react with adesilylation agent.

As the reaction solvent, THF, chloroform, dichloromethane, toluene,water, methanol, and the like may be used alone or as a mixture thereof.Examples of the desilylation agent include tetrabutylammonium fluoride(TBAF), sodium fluoride, hydrofluoric acid, and the like. The reactionmay be carried out by increasing the reaction pH by adding an acid, suchas acetic acid, hydrochloric acid or the like. The desilylation agent isused in an amount of 0.1 equivalent or more, preferably 1 to 10equivalents, based on compound (Ie). The reaction is carried out at atemperature of −20 to 50° C., and the reaction completes after 5 minutesto 24 hours.

Production method 6

Compound (Ih) can be prepared by ring-opening the epoxide of compound(Ig) into a halohydrin or the like.

[In the above reaction formula, R^(1a), R^(2a) and R³ have the samemeaning as defined above; X^(a) represets halogen; and R^(4a) representshydrogen, formyl, or —SO—Z (wherein Z has the same meaning as definedabove).]

Step 6-1

A member of compound (Ih) in which R^(4a) is hydrogen can be prepared byallowing compound (Ig) to react with an acid (for example, hydrogenchloride, hydrogen bromide, or the like) or a Lewis acid (for example,titanium tetrachloride, or the like).

As the solvent, dioxane, THF, ether, chloroform, dichloromethane, DMF,acetonitrile, methanol, ethyl acetate, and the like may be used eitheralone or as a mixture thereof. The acid or Lewis acid is used in anamount of 1 equivalent or more, preferably 1 to 10 equivalents, based oncompound (Ig). The reaction is carried out at a temperature of −20 to40° C., preferably 0 to 40° C., and the reaction completes after 10minutes to 48 hours.

Step 6-2

A member of compound (Ih) in which R^(4a) is formyl can be prepared byallowing compound (Ig) to react with phosphorous oxychloride orphosphorous oxybromide in DMF. Phosphorous oxychloride or phosphorousoxybromide is used in an amount of 1 equivalent or more, preferably 2 to5 equivalents, based on compound (Ig). The reaction is carried out at atemperature of −10 to 40° C., preferably 0 to 40° C., and the reactioncompletes after 1 to 48 hours.

Step 6-3

A dimer compound as a member of compound (Ih) in which R^(4a) is —SO—Z(wherein Z has the same meaning as defined above) can be prepared byallowing compound (Ig) to react with thionyl chloride or thionylbromide. As the solvent, DMF, chloroform, dichloromethane, dimethylsulfoxide (DMSO), acetonitrile, and the like may be used either alone oras a mixture thereof. Thionyl chloride or thionyl bromide is used in anamount of 1 equivalent or more, preferably 2 to 10 equivalents, based oncompound (Ig). The reaction is carried out at a temperature of −10 to40° C., preferably 0 to 40° C., and the reaction completes after 1 to 48hours.

Production method 7

Compound (Ij) which is a derivative of compound (I) in which at leastone of R¹ and R² is substituted with tert-butyldimethylsilyl ortert-butyldiphenylsilyl can be prepared from compound (Ii) by thefollowing step.

(In the above reaction formula, R³, R⁴, and X have the same meaning asdefined above; R^(1e) and R^(2e) represent both hydrogen, or onerepresents hydrogen and the other represents alkanoyl or alkenoyl; andR^(1f) and R^(2f) represent groups in which at least one hydrogen ofeither of the above R^(1e) and R^(2e) is substituted withtert-butyldimethylsily or tert-butyldiphenylsilyl.)

Step 7

Compound (Ij) can be prepared by allowing compound (Ii) to react withtert-butyl(chloro)dimethylsilane or tert-butylchlorodiphenylsilane inthe presence of a base.

As the solvent, chloroform, dichloromethane, ether, THF, acetone, DMF,acetonitrile, and the like are used either alone or a mixture thereof.As the base, amines (for example, pyridine, imidazole, triethylamine,diisopropylethylamine, or the like) are used.Tert-butyl(chloro)dimethylsilane or tert-butylchlorodiphenylsilane isused in an amount of 1 equivalent or more, preferably 1 to 10equivalents, based on compound (ii). The base is used in an amount of 1equivalent or more, preferably 1 to 10 equivalent, based ontert-butyl(chloro)dimethylsilane or tert-butylchlorodiphenylsilane. Thereaction is carried out at a temperature of −20 to 50° C., preferably 10to 40° C., and the reaction completes after 10 minutes to 24 hours.

Production method 8

Compound (Im) in which at least one hydrogen of any one of R¹, R² and R⁴in compound (I) is substituted with alkanoyl or alkenoyl can be preparedby carrying out acylation of the following compound (Ik).

(In the above reaction formula, R³ and X have the same meaning asdefined above; at least one of R^(1g), R^(2g) and R^(4b) representshydrogen; and R^(1h), R^(2h) and R^(4c) represent groups in which atleast one hydrogen of the above R^(1g), R^(2g) and R^(4b) is substitutedwith alkanoyl or alkenoyl.)

Step 8

Compound (Im) can be prepared by allowing compound (Ik) to react with 1equivalent or more, preferably 1 to 100 equivalents, or an acid halide,an acid anhydride, a mixed acid anhydride containing the alkanoyl oralkenoyl or interest, or the like, in the presence of a base.

As the solvent, DMF, DMSO, chloroform, dichloromethane, toluene, and thelike may be used either alone or as a mixture thereof. An optionalhydroxyl group can be modified by optionally carrying out introductionand elimination of a protecting group of the hydroxyl group, and it ispossible to modify a plurality of hydroxyl groups at the same time. Asthe base, pyridine, triethylamine, N,N-dimethylaniline,N,N-diethylaniline, or the like is used in an amount of 1 equivalent ormore, preferably 1 to 200 equivalents, based on compound (Ik). It ispossible to use a base (for example, pyridine, or the like) also as thesolvent. Additionally, the reaction can be accelerated by adding DMAP orthe like in an amount of 0.1 to 4 equivalents based on compound (Ik).The reaction is carried out at a temperature of −20 to 50° C., and thereaction completes after 5 minutes to 24 hours.

In the production of compound (I), conversion of the functional group ofR¹, R², R³, R⁴ or X can be carried out not only by the above steps butalso by known methods [for example, Comprehensive OrganicTransformations, R. C. Larock (1989)].

Isolation and purification of the products of the above methods can becarried out by carrying out optional combinations of techniquesgenerally used in organic syntheses (e.g., filtration, extraction,washing, drying, concentration, crystallization, various types ofchromatography, and the like). The intermediates may be used in thesubsequent reactions without purification.

If a salt of compound (I) is prepared, the salt of compound (I) can bepurified as such when it can be prepared; or, when the compound isprepared in its free form, its salt can be formed by dissolving orsuspending it in an appropriate solvent and adding an acid or basethereto.

Also, compound (I) or pharmacologically acceptable salts thereof mayexist in the form of addition products with water or various solvents,and these addition products are also included in the present invention.Examples of compound (I) are shown in Table 1.

TABLE 1 Specific examples of compound (I)

Compound R³  1

 2

 3

 4

 5 CH₂CONH(CH₂)₂N(CH₂CH₃)₂  6 CH₂CONH(CH₂)₂OH  7 CH₂CON[(CH₂)₂OH]₂  8CH₂CONHCH₂CO₂CH₃  9 CH₂CONHNH₂ 10 CH₂CONHNHCONHC₆H₅ 11

12

13

14

15

16 CH₂CONH(CH₂)₉CH₃ 17

18

19

20

21

22

23

24

25

26

27

28 CH₂CONHC₆H₅ 29

30

31

32

33 CH₂CONHN(CH₃)₂ 34

35 CH₂CONHNHC₅H₆ 36

37

38

39

40

41 CH₂CO₂(CH₂CH₂O)₆CH₃ 42 CH₂CO₂(CH₂CH₂O)₃CH₃ 43

44

45

46

47

48

49

50

51

52

53

54

55

56

57

58

59

60

61

62

63

64

65

66

67

68

69

70

71

72

73 CO₂CH₂CH₃ 74 CONHCH₃ 75 COCH₃ 76 C₆H₅

Next, pharmacological activities of typical examples of compound (I) aredescribed by the following test examples.

TEST EXAMPLE 1

Inhibition test of intracellular tyrosine kinase

SR-3Y1 cells were cultured at 37° C. for 15 hours in an atmosphere of 5%carbon dioxide, using Dulbecco's modified Eagle's medium (DMEM)containing 10% fetal calf serum (FCS), to which each radicicolderivative to be tested had been added in varied concentration. The thuscultured cells were lysed at 4° C. for 20 minutes in a cooled buffer forlysis use (50 mM Tris HCl, pH 7.5, 150 mM sodium chloride (NaCl), 1%Triton X-100, 0.1% sodium dodecyl sulfate (SDS), 1% sodium deoxycholate,2 mM ethylenediaminetetraacetic acid (EDTA), 1 mM phenylmethanesulfonylfluoride (PMSF), 20 μM leupeptin, 0.15 unit/ml aprotinin, 1 mM sodiumorthovanadate (Na₃VO₄) and then centrifuged at 20,000 G for 30 minutes.After measuring protein concentration in the resulting supernatantfluid, samples were adjusted to the same protein quantity per lane tocarry out separation of the protein by SDS-PAGE. The thus separatedprotein samples were transferred onto a nitrocellulose membrane to whichwere subsequently added a mouse polyclonal phosphotyrosine antibodyMX-pTYR (Kyowa Medex Co., Ltd.) as a first antibody and a horseradishperoxidase-conjugated mouse IgG antibody (BIO-RAD Co.) as a secondantibody, thereby reacting them with the protein samples on themembrane. Detection was carried out using ECL reagent (Amersham Co.),and the amount of tyrosine-phosphorylated protein was determined byscanning the density of bands prepared on an X-ray film. The activity ofradicicol derivatives to inhibit tyrosine phosphorylation can be shownas a concentration (IC₅₀) of each derivative by which the ratio oftyrosine-phosphorylated protein is reduced to half in comparison with acontrol to which the drug is not added.

The results are shown in Table 2.

TABLE 2 Inhibitory activity of intracellular tyrosine kinase CompoundIC₅₀ (μM) Radicicol 0.37  1 0.02  3 0.21 73 0.13

According to Table 2, the test compounds show clearly stronger action toinhibit intracellular tyrosine kinase activity than radicicol, andtherefore, compound (I) is useful as a tyrosine kinase inhibitor.

TEST EXAMPLE 2

Inhibition test on the growth of rat normal fibroblast cell line 3Y1-Band its v-src oncogene transformed cell line SR-3Y1

The cells were inoculated into a 96 well microplate (#167008,manufactured by Nunc) in an amount of 1,000 cells per well andpre-cultured at 37° C. for 24 hours in a 5% carbon dioxide gas incubatorusing Dulbecco's modified Eagle's medium (DMEM) which had beensupplemented with 10% fetal calf serum (FCS). Next, a DMSO solution ofeach test compound which has been adjusted to 10 mM was serially dilutedwith the culturing medium and added to the wells in 50 μl portions.Thereafter, the culturing was continued at 37° C. for 72 hours in the 5%carbon dioxide gas incubator. Five hours before completion of theculturing, 3-(4,5-dimethylthiazo-2-yl)-2,5-diphenyltetrazolium bromide(manufactured by Sigma, hereinafter referred to as “MTT”) which had beendissolved in the culturing medium to a final concentration of 1 mg/μlwas dispensed into the wells in 50 μl portions. After completion of theculturing, DMSO was dispensed into the wells in 150 ml portions, and theplate was vigorously stirred using a plate mixer to dissolveMTT-formazan crystals completely. Thereafter, absorbance at 550 nm wasmeasured using a microplate reader MTF-32 (manufactured by CoronaDenki). The cell growth inhibition activity was expressed by 50%inhibition concentration (IC₅₀).

The results are shown in Table 3.

TABLE 3 Growth inhibition activity upon rat normal fibroblast cell line3Y1-B and its v-src oncogene transformed cell line SR-3Y1 Growthinhibition activity IC₅₀ (μM) Compound 3Y1-B SR-3Y1 Radicicol 0.7800.042  1 0.008 <0.004 21 0.032 0.018 27 0.041 0.010 44 0.069 0.012 500.120 0.021 53 0.008 <0.004 55 0.009 <0.004 67 0.140 0.018 69 0.0080.004 72 0.055 0.010 74 0.072 0.027 76 0.110 0.026

According to Table 3, the test compounds showed stronger cell growthinhibition activity upon SR-3Y1 than that upon 3Y1-B and stronger cellgrowth inhibition activity than that of radicicol upon SR-3Y1. Becauseof these results, compound (I) is useful as an antitumor agent.

TEST EXAMPLE 3

Antitumor test on nude mouse-transplanted human breast cancer MX-1 solidtumor

From a tumor lump of a human breast cancer cell line MX-1 subcultured innude mice (BALB/c nu/nu mice: CLEA Japan), a portion showing good growthwas selected and cut into a 2 mm square fragment which was thentransplanted under the abdominal side skin of each male nude mouse of 7to 9 weeks of age using a trocar. The tumor size was measured on the13th day after the tumor transplantation to select properly growingtumors having a tumor volume of 100 to 300 mm³ (calculated by acalculation formula of “major axis×minor axis²×½”), the mice wereoptionally grouped into 5 animals per group, and then each test compoundwhich had been dissolved in a 7.5% cremohor EL (manufactured bySigma)/5% dimethylacetamide (DMA)/87.5% physiological saline solutionwas administered to the mice by intravenous injection at a dosage of0.05 ml (100 mg/kg) per day, once a day for 5 days. The antitumoractivity of each test compound was expressed by a ratio (T/C) of thetumor volume (T) in the test drug-administered group to the tumor volume(C) in the control group on the 12th or 14th day after administration ofthe test compound.

The results are shown in Table 4.

TABLE 4 Antitumor activity against human breast cancer MX-1 solid tumorinoculated in nude mouse Day measured (after Compound T/C (%)administration of test compound)  1  3 14 51 33 14 53 46 12 69  4 12

According to Table 4, the test compounds show excellent antitumoractivity, and therefore, compound (I) is useful as an antitumor agent.

TEST EXAMPLE 4

Effect of decreasing intracellular Raf-1 protein quantity and Erk2phosphorylation inhibition activity

Activated K-ras gene-introduced rat kidney epithelial cell line KNRK 5.2was cultured at 37° C. for 40 hours in an atmosphere of 5% carbondioxide gas using Dulbecco's modified Eagle's medium (DMEM) which wassupplemented with 10% fetal calf serum (FCS) and to which was added eachradicicol derivative at respective test concentration. The resultingcells were lysed for 30 minutes at 4° C. in a cooled buffer for lysisuse [50 mM HEPES NaOH, pH 7.4, 250 mM sodium chloride (NaCl), 1 nMethylenediaminetetraacetic acid (EDTA), 1% Nonidet P-40 (NP40), 1 mMdithiothreitol (DTT), 1 mM phenylmethylsulfonyl fluoride (PMSF), 5 μg/mlleupeptin, 2 mM sodium orthovanadate (Na₃VO₄), 1 mM sodium fluoride(NaF), 10 mM β-glycerophosphate] and then centrifuged at 30,000 G for 10minutes. The protein content of the thus prepared supernatant fluids wasmeasured to prepare samples having the same protein quantity for eachlane, and then separation of proteins was carried out by SDS-PAGE. Thethus separated protein samples were transferred on a polyvinylidenedifluoride (PVDF) membrane, and then anti-phosphorylation MAPK antibody(anti-phospho MAPK, manufactured by New England Biolabs), anti-Erk2antibody (anti-Erk2, manufactured by Upstate Biotechnology) andanti-Raf-1 antibody (anti-Raf-1(C-12), manufactured by Santa CruzBiotechnology) were added thereto as primary antibodies and allowed toreact with the proteins on the membrane. Thereafter, a horseradishperoxidase-labeled secondary antibody (anti-rabbit Ig antibody oranti-mouse Ig antibody, manufactured by Amersham) capable of reactingwith respective primary antibodies was added thereto as the secondaryantibody to carry out the reaction. Detection was carried out using ECLreagent (manufactured by Amersham), and the amount of phosphorylatedErk2 protein, total Erk2 protein and Raf-1 protein was determined bycarrying out density scanning of the bands generated on the X-ray film.The Erk2 phosphorylation inhibition activity of radicicol derivatives isdetermined by calculating the ratio of phosphorylated Erk2 protein(phosphorylated Erk2 protein/total Erk2 protein) based on the resultsprepared from the samples of respective drug concentrations, which isexpressed as the concentration of each derivative (IC₅₀) by which theratio becomes half in comparison with the case in which the drug is notadded. Also, the Raf-1 protein decreasing action is examined bycalculating the ratio of Raf protein to the amount of Erk2 protein whichdoes not cause changes in the protein quantity by the drug-treatment(Raf-1 protein/total Erk2 protein) based on the results prepared fromthe samples having respective drug concentrations, which is expressed asthe concentration of each derivative (IC₅₀) by which the ratio becomeshalf in comparison with the case in which the drug is not added.

The results are shown in Table 5.

TABLE 5 Effect of decreasing intracellular Raf-1 protein quantity andErk2 phosphorylation inhibition activity Raf-1 protein quantity Erk2phosphorylation Compound decrease: IC₅₀ (μM) inhibition: IC₅₀ (μM) 500.34 0.35 53 0.38 0.07 64 0.19 0.11 69 0.12 0.06

According to Table 5, the test compounds showed effect of decreasingintracellular Raf-1 protein quantity and Erk2 phosphorylation inhibitionactivity.

Compound (I) or a pharmacologically acceptable salt thereof isadministered orally or parenterally as it is or in the form of apharmaceutical composition. Examples of the dosage form of such apharmaceutical composition include tablets, pills, powders, granules,capsules, suppositories, injections, drip infusions, and the like.

These dosage forms can be prepared by employing generally known methodsand may contain various fillers, lubricants, binders, disintegrators,suspending agents, tonicity agents, emulsifying agents, absorptionenhancers, and the like.

Examples of carriers to be used in the pharmaceutical compositioninclude water, distilled water for injection use, physiological saline,glucose, fructose, sucrose, mannitol, lactose, starch, corn starch,cellulose, methyl cellulose, carboxymethyl cellulose, hydroxypropylcellulose, alginic acid, talc, sodium citrate, calcium carbonate,calcium hydrogenphosphate, magnesium stearate, urea, silicone resin,sorbitan fatty acid ester, glycerol fatty acid ester and the like, whichmay be optionally selected according to the kind of the pharmaceuticalpreparation.

Although the dosage and the number of administration times for thepurposes may vary depending on the intended therapeutic effect,administration method, treating period, age, body weight, and the like,it may be administered generally in a dose of 0.01 to 5 mg/kg per dayper adult.

BEST MODE OF CARRYING OUT THE INVENTION

Examples and Reference Examples are shown below. The NMR data shown inExamples and Reference Examples are values obtained by measuring at 270MHz, and the number of protons observed, multiplicity and couplingconstant (unit, Hz) are shown in that order in parentheses after the δvalue of each signal.

TBS and Boc shown in the following structural formulae and Tables meanstert-butyldimethylsilyl and tert-butoxycarbonyl, respectively.

EXAMPLE 1

Compound 1

(1—1)

A 1.50 g (4.11 mmol) portion of radicicol was dissolved in 5 ml ofpyridine, and the solution was mixed with 1.00 g (9.15 mmol) ofaminooxyacetic acid hemihydrochloride and stirred at room temperaturefor 20 hours and then at 60° C. for 1.5 hours. The solvent wasevaporated under reduced pressure, and the resulting residue waspurified by silica gel column chromatography (chloroform/methanol=49/1)to obtain 692 mg (yield, 38%) of a compound (K). The thus preparedcompound (K) was found to be a mixture of oxime-based isomers (about3:1) according to ¹H-NMR.

FAB-MS m/z: 438 [M+H]⁺

Major component: ¹H-NMR (CD₃OD) δ(ppm): 7.27 (1H, dd, 16.1, 11.2 Hz),6.82 (1H, d, 16.1 Hz), 6.42 (1H, s), 6.17 (1H, dd, 11.2, 10.5 Hz), 5.61(1H, dd, 10.5, 3.4 Hz), 5.31 (1H, m), 4.64 (2H, m), 3.91 (1H, d, 16.4Hz), 3.82 (1H, d, 16.4 Hz), 3.34 (1H, m), 3.02 (1H, m), 2.42 (1H, m),1.60 (1H, ddd, 14.4, 9.0, 4.2 Hz), 1.53 (3H, d, 6.6 Hz).

(1-2)

A 230 mg (0.525 mmol) portion of compound (K) was dissolved in 3 ml ofDMF, and the solution was mixed with 121 mg (0.788 mmol) of HOBt, 151 mg(0.788 mmol) of EDCI and 0.078 ml (0.788 mmol) of piperidine and stirredat room temperature for 23 hours and 40 minutes. The reaction solutionwas mixed with a 0.01 M phosphate buffer of pH 7 and then extracted withethyl acetate. The ethyl acetate layer was washed with saturated brineand dried with anhydrous sodium sulfate, and then the solvent wasevaporated under reduced pressure. The resulting residue was purified bysilica gel column chromatography (chloroform/methanol=50/1) to obtain63.6 mg (yield, 24%) of compound 1. The thus prepared compound 1 wasfound to be a mixture of oxime-based isomers (about 4:1) according to¹H-NMR.

FAB-MS m/z: 505 [M⇄H]⁺

Major component: ¹H-NMR (CD₃OD) δ(ppm): 7.27 (1H, dd, 15.8, 10.9 Hz),6.80 (1H, d, 16.3 Hz), 6.44 (1H, s), 6.17 (1H, dd, 11.9, 10.9 Hz), 5.61(1H, dd, 10.9, 3.5 Hz), 5.31 (1H, m), 4.80 (2H, s), 3.93 (1H, d, 15.9Hz), 3.82 (1H, d, 16.3 Hz), 3.40-3.60 (4H, m), 3.34 (1H, m), 3.02 (1H,m), 2.49 (1H, ddd, 14.4, 3.5, 3.5 Hz), 1.60-1.80 (7H, m), 1.52 (3H, d,6.4 Hz).

EXAMPLE 2

Compound 2

According to (1-2) described in Example 1, 109 mg (yield, 49%) ofcompound 2 was prepared from 200 mg (0.457 mmol) of compound (K), 77 mg(0.503 mmol) of HOBt, 96 mg (0.503 mmol) of EDCI and 0.042 ml (0.503mmol) of pyrroridine. The thus prepared compound 2 was found to be amixture of oxime-based isomers (about 3:1) according to ¹H-NMR.

FAB-MS m/z: 491 [M+H]⁺

Major component: ¹H-NMR (DMSO-d₆) δ(ppm): 10.34 (1H, br s), 10.00 (1H,br s), 7.14 (1H, dd, 16.0, 11.4 Hz), 6.74 (1H, d 15.8 Hz), 6.51 (1H, s),6.23 (1H, dd, 11.2 10.9 Hz), 5.63 (1H, dd, 10.4, 3.5 Hz), 5.14 (1H, m),4.68 (2H, s), 3.80 (1H, d, 1.58 Hz), 3.51 (1H, d, 15.2 Hz), 3.27-3.54(4H, m), 3.05 (1H, m), 2.44 (1H, m), 170-1.91 (5H, m), 1.43 (3H, d, 6.3Hz).

EXAMPLE 3

Compound 3

According to (1-2) described in Example 1, 42 mg (yield, 12%) ofcompound 3 was prepared from 300 mg (0.685 mmol) of compound (K), 155 mg(0.753 mmol) of DCC, 87 mg (0.753 mmol of HONSu and 0.090 ml (0.753mmol) of morpholine. The thus prepared compound 3 was found to be amixture of oxime-based isomers (about 4:1) according to ¹H-NMR.

FAB-MS m/z: 507 [M+H]⁺

Major component: ¹H-NMR (CD₃OD) δ(ppm): 7.28 (1H, dd, 15.8, 11.4 Hz),6.78 (1H, d, 16.3 Hz), 6.42 (1H, s), 6.17 (1H, dd, 11.4, 10.4 Hz), 5.62(1H, dd, 10.4 3.0 Hz), 5.30 (1H, m), 4.82 (2H, s), 3.87 (1H, d, 15.8Hz), 3.82 (1H, d, 16.3 Hz), 3.57-3.71 (8H, m), 3.34 (1H, m), 3.05 (1H,m), 2.42 (1H, ddd, 14.4, 4.0, 3.5 Hz), 1.94 (1H, m), 1.52 (3H, d, 6.9Hz).

EXAMPLE 4

Compound 4

According to (1-2) described in Example 1, 24 mg (yield, 20%) ofcompound 4 was prepared from 100 mg (0.288 mmol) of compound (K), 52 mg(0.251 mmol) of DCC, 29 mg (0.251 mmol) of HONSu and 0.028 ml (0.251mmol) of 1-methylpiperazine. The thus prepared compound 4 was found tobe a mixture of oxime-based isomers (about 4:1) according to ¹H-NMR.

FAB-MS m/z: 520 [M+H]³⁰

Major component: ¹H-NMR (CD₃OD) δ(ppm): 7.01 (1H, dd, 15.8, 11.4 Hz),6.69 (1H, d, 15.8 Hz), 6.33 (1H, s), 6.07 (1H, t, 10.9 Hz), 5.52 (1H,dd, 10.4, 4.0 Hz), 5.20 (1H, m), 4.72 (2H, s), 3.84 (1H, d, 16.3 Hz),3.72 (1H, d, 16.3 Hz), 3.41-3.55 (4H, m), 3.25 (1H, m), 2.92 (1H, m),2.28-2.41 (5H, m), 2.22 (3H, s), 1.50 (1H, m), 1.42 (3H, d, 6.4 Hz).

EXAMPLE 5

Compound 5

According to (1-2) described in Example 1, 46 mg (yield, 37%) ofcompound 5 was prepared from 100 mg (0.288 mmol) of compound (K), 52 mg(0.251 mmol) of DCC, 29 mg (0.251 mmol) of HONSu and 0.035 ml (0.251mmol) of N,N-diethylethylenediamine. The thus prepared compound 5 wasfound to be a mixture of oxime-based isomers (about 3:1) according to¹H-NMR.

FAB-MS m/z: 537 [M+H]⁺

Major component: ¹H-NMR (CD₃OD) δ(ppm): 7.30 (1H, dd, 15.8, 11.4 Hz),6.84 (1H, d, 16.3 Hz), 6.39 (1H, s), 6.18 (1H, t, 10.9 Hz), 5.63 (1H,dd, 10.9, 3.5 Hz), 5.30 (1H, m), 3.96 (2H, br), 3.44-3.52 (2H, m), 3.36(1H, m), 3.00 (1H, m), 2.77-2.82 (6H, m), 2.60 (1H, m), 1.67 (1H, m),1.51 (3H, d, 6.4Hz), 1.07-1.19 (6H, m).

EXAMPLE 6

Compound 6

According to (1-2) described in Example 1, 87 mg (yield, 40%) ofcompound 6 was prepared from 200 mg (0.456 mmol) of compound (K), 88 mg(0.457 mmol) of EDCI, 56 mg (0.457 mmol) of DMAP and 25 mg (0.457 mmol)of 2-aminoethanol. The thus prepared compound 6 was found to be amixture of oxime-based isomers (about 5:1) according to ¹H-NMR.

Major component: ¹H-NMR (CD₃OD) δ(ppm): 7.30 (1H, dd, 15.8, 11.4 Hz),6.85 (1H, d, 16.3 Hz), 6.44 (1H, s), 6.19 (1H, t, 10.9 Hz), 5.63 (1H,dd, 10.9, 3.0 Hz), 5.31 (1H, m), 4.58 (2H, s), 3.96 (1H, d, 16.3 Hz),3.85 (1H, d, 16.3 Hz), 3.54-3.70 (2H, m), 3.31-3.40 (2H, m), 3.31 (1H,m), 3.02 (1H, m), 2.43 (1H, m), 1.61 (1H, m), 1.52 (3H, d, 6.4 Hz).

EXAMPLE 7

Compound 7

According to (1-2) described in Example 1, 45 mg (yield, 13%) ofcompound 7 was prepared from 300 mg (0.685 mmol) of compound (K), 132 mg(0.685 mmol) of EDCI, 94 mg (0.685 mmol) of DMAP and 97 mg (0.685 mmol)of 2,2′-iminodiethanol hydrochloride. The thus prepared compound 7 wasfound to be a mixture of oxime-based isomers (about 5:1) according to¹H-NMR.

Major component: ¹H-NMR (CD₃OD) δ(ppm): 7.26 (1H, dd, 15.8, 10.9 Hz),6.83 (1H, d, 15.8 Hz), 6.42 (1H, s), 6.17 (1H, dd, 11.4, 10.4 Hz), 5.60(1H, dd, 10.4, 3.5 Hz), 5.29 (1H, m), 4.91 (2H, s), 3.91 (1H, d, 15.8Hz), 3.80 (1H, d, 15.8 Hz), 3.71-3.90 (4H, m), 3.52-3.59 (4H, m), 3.34(1H, m), 3.00 (1H, m), 2.42 (1H, ddd, 14.8, 3.5, 3.5 Hz), 1.60 (1H, m),1.52 (3H, d, 6.4 Hz).

EXAMPLE 8

Compound 8

According to (1-2) described in Example 1, 89 mg (yield, 38%) ofcompound 8 was prepared from 200 mg (0.456 mmol) of compound (K), 87 mg(0.456 mmol) of EDCI, 56 mg (0.457 mmol) of DMAP and 63 mg (0.502 mmol)of glycine methyl ester hydrochloride. The thus prepared compound 8 wasfound to be a mixture of oxime-based isomers (about 4:1) according to¹H-NMR.

FAB-MS m/z: 509 [M+H]⁺

Major component: ¹NMR (CD₃OD) δ(ppm): 7.30 (1H, dd, 16.3, 11.9 Hz), 6.87(1H, d, 15.8 Hz), 6.44 (1H, s), 6.20 (1H, dd, 10.4, 9.4 Hz), 5.63 (1H,dd, 10.4, 4.0 Hz), 5.31 (1H, m), 4.85 (2H, s), 4.02 (1H, d, 2.0 Hz),3.96 (1H, d, 15.8 Hz), 3.83 (1H, d, 15.8 Hz), 3.73 (3H, s), 3.36 (1H,m), 3.03 (1H, m), 2.44 (1H, ddd, 14.3, 3.5, 3.5 Hz), 1.65 (1H, m), 1.53(3H, d, 6.4 Hz).

EXAMPLE 9

Compound 9

A 46 mg (0.150 mmol) portion of compound (K) was dissolved in 1.5 ml oftetrahydrofuran, and the solution was mixed with 23 mg (0.200 mmol) ofHOBt, 2.7 mg (0.022 mmol) of DMAP and 44 mg (0.228 mmol) of EDCI andstirred at room temperature for 16 hours. The resulting precipitate wasseparated by filtration, and the solvent was evaporated under reducedpressure. The thus prepared residue was dissolved in 1.5 ml oftetrahydrofuran, and the solution was mixed with 0.100 ml (0.720 mmol)of triethylamine and 0.050 ml (1.030 mmol) of hydrazine hydrate andstirred at room temperature for 12 hours. The reaction solution wasmixed with ethyl acetate, washed with a saturated ammonium chlorideaqueous solution and dried with anhydrous sodium sulfate, and then thesolvent was evaporated under reduced pressure. The resulting residue waspurified by silica gel column chromatography (chloroform/methanol=24/1)to obtain 33 mg (yield, 48%) of compound 9. The thus prepared compound 9was found to be a mixture of oxime-based isomers (about 3:1) accordingto ¹H-NMR.

FAB-MS m/z: 452 [M+H]⁺

Major component: ¹H-NMR (CD₃OD) δ(ppm): 7.28 (1H, dd, 16.1, 11.3 Hz),6.83 (1H, d, 16.1 Hz), 6.43 (1H, s), 6.19 (1H, dd, 11.3, 10.7 Hz), 5.62(1H, dd, 10.7, 3.7 Hz), 5.30 (1H, m), 3.94 (1H, d, 16.1 Hz), 3.79 (1H,d, 16.1 Hz), 3.31 (1H, m), 3.02 (1H, m), 2.43 (1H, m), 1.59 (1H, m),1.52 (3H, d, 6.5 Hz).

EXAMPLE 10

Compound 10

According to (1-2) described in Example 1, 35 mg (yield, 27%) ofcompound 10 was prepared from 100 mg (0.228 mmol) of compound (K), 44 mg(0.228 mmol) of EDCI and 35 mg (0.228 mmol) of 4-phenylsemicarbazide.The thus prepared compound 10 was found to be a mixture of oxime-basedisomers (about 5:1) according to ¹H-NMR.

Major component: ¹H-NMR (CD₃OD) δ(ppm): 7.23-7.42 (5H, m), 7.02 (1H, t,7.4 Hz), 6.88 (1H, d, 15.8 Hz), 6.45 (1H, s), 6.18 (1H, t, 10.9 Hz),5.62 (1H, dd, 10.9, 3.5 Hz), 5.31 (1H, m), 4.73 (2H, s), 3.97 (1H, d,16.3 Hz), 3.86 (1H, d, 16.3 Hz), 3.36 (1H, m), 3.01 (1H, m), 2.42 (1H,ddd, 14.3, 3.5, 3.5 Hz), 1.61 (1H, m), 1.51 (3H, d, 6.4 Hz).

EXAMPLES 11-37

Compounds 11 to 38 were prepared from compound (K) according to (1-2)described in Example 1.

EXAMPLE 11

Compound 11

Isomer ratio: about 10:1

FAB-MS m/z: 519 [M+H]⁺

Major component: ¹H-NMR (CDCl₃) δ(ppm): 10.78 (1H, br), 7.86 (1H, br s),7.14 (1H, dd, 15.8, 11.6 Hz), 6.75 (1H, d, 15.8 Hz), 6.60 (1H, s), 6.09(1H, dd, 11.6, 10.2 Hz), 5.60 (1H, dd, 10.6, 3.0 Hz), 5.47 (1H, m), 4.85(1H, d, 13.9 Hz), 4.79 (1H, d, 13.9 Hz), 4.69 (1H, br), 3.98 (1H, br),3.37-3.56 (4H, m), 3.16 (1H, br), 2.94 (2H, dd, 8.6, 2.6, 2.3 Hz), 2.31(1H, ddd, 15.2, 3.6, 3.6 Hz), 1.95 (1H, ddd, 15.2, 8.9, 4.0 Hz), 1.74(2H, br), 1.53 (3H, d, 6.9 Hz), 1.49-1.58 (2H, br), 1.20-1.29 (4H, br).

EXAMPLE 12

Compound 12

Isomer ratio: about 3:1

FAB-MS m/z: 519 [M+H]⁺

Major component: ¹H-NMR (CDCl₃) δ(ppm): 10.99 (1H, br), 8.00 (1H, br),7.16 (1H, m), 6.73 (1H, d, 16.2 Hz), 6.59 (1H, s), 6.11 (1H, dd, 10.6,10.2 Hz), 5.62 (1H, br d, 9.6 Hz), 5.48 (1H, m), 4.80 (2H, s), 4.67 (1H,d, 12.2 Hz), 4.54 (2H, br), 4.00 (1H, br), 3.73-3.89 (2H, br), 3.17 (1H,br), 3.04 (1H, m), 2.50-2.65 (2H, m), 2.32 (1H, ddd, 15.2, 3.6, 3.3 Hz),1.93 (1H, ddd, 18.8, 9.2, 4.6 Hz), 1.58-1.70 (2H, m), 1.54 (3H, d, 6.9Hz), 1.04-1.19 (2H, m), 0.94 (3H, d, 6.3 Hz).

EXAMPLE 13

Compound 13

Isomer ratio: about 3:1

FAB-MS m/z: 521 [M+H]⁺

Major component: ¹H-NMR (CDCl₃) δ(ppm): 7.16 (1H, m), 6.70 (1H, d, 16.2Hz), 6.57 (1H, s), 6.11 (1H, dd, 10.6, 10.2 Hz), 5.63 (1H, br d, 11.2Hz), 5.48 (1H, m), 4.80 (2H, s), 4.63 (1H, br), 3.95 (3H, br), 3.76 (1H,br), 3.19-3.47 (3H, m), 2.96 (1H, br), 2.33 (1H, m), 1.90 (1H, m), 1.54(3H, d, 6.6 Hz), 1.20-1.28 (4H, m).

EXAMPLE 14

Compound 14

Isomer ratio: about 8:1

FAB-MS m/z: 588 [M+H]⁺

Major component: ¹H-NMR (CDCl₃+CD₃OD) δ(ppm): 7.01 (1H, dd, 16.0, 11.0Hz), 6.62 (1H, d, 15.8 Hz), 6.34 (1H, s), 6.06 (1H, dd, 11.6, 9.9 Hz),5.46 (1H, br d, 10.6 Hz), 5.34 (1H, br), 4.68 (2H, s), 4.55 (1H, d, 17.8Hz), 3.96 (1H, br), 3.20 (1H, br), 2.82-2.99 (2H, m), 2.60 (8H, br),2.25 (1H, br d, 11.6 Hz), 1.89 (2H, br), 1.70-1.80 (4H, br), 1.61 (4H,br), 1.44 (3H, d, 6.6 Hz).

EXAMPLE 15

Compound 15

Isomer ratio: about 3:1

FAB-MS m/z: 548 [M+H]⁺

Major component: ¹H-NMR (CDCl₃) δ(ppm): 7.13 (1H, dd, 16.0, 11.4 Hz),6.64 (1H, d, 16.2 Hz), 6.41 (1H, s), 6.06 (1H, dd, 11.9, 10.2 Hz), 5.57(1H, dd, 10.2, 3.0 Hz), 5.37 (1H, m), 4.70 (2H, s), 4.33-4.52 (2H, m),3.91-4.01 (2H, m), 3.17 (1H, br), 2.80-3.08 (2H, m), 2.66 (1H, m),2.24-2.40 (2H, m), 1.54-1.84 (5H, br), 1.47 (3H, d, 6.6 Hz).

EXAMPLE 16

Compound 16

Isomer ratio: about 4:1

FAB-MS m/z: 577 [M+H]⁺

Major component: ¹H-NMR (CDCl₃) δ(ppm): 10.71 (1H, br), 8.83 (1H, br),7.23 (1H, dd, 16.0, 11.4 Hz), 6.66 (1H, d, 16.2 Hz), 6.60 (1H, s), 6.41(1H, t, 5.8 Hz), 6.13 (1H, dd, 11.2, 10.9 Hz), 5.67 (1H, dd, 10.2, 3.0Hz), 5.47 (1H, m), 4.66 (1H, br), 4.59 (2H, s), 4.02 (1H, d, 15.2 Hz),3.25-3.35 (2H, m), 3.20 (1H, br, 2.95 (1H, m), 2.33 (1H, m), 1.95 (1H,m), 1.54 (3H, d, 6.6 Hz), 1.51 (2H, br), 1.21 (14H, br), 0.83 (3H, t,5.6 Hz).

EXAMPLE 17

Compound 17

Isomer ratio: about 13:1

FAB-MS m/z: 513 [M+H]⁺

Major component: ¹H-NMR (CDCl₃) δ(ppm): 10.77 (1H, br), 7.25 (1H, dd,16.2, 11.2 Hz), 7.02 (1H, br), 6.68 (1H, d, 16.2 Hz), 6.61 (1H, s), 6.51(1H, t, 5.9 Hz), 6.17 (1H, dd. 11.2, 10.6 Hz), 5.71 (1H, dd, 10.2, 3.3Hz), 5.51 (1H, m), 4.73 (1H, d, 15.8 Hz), 4.62 (2H, s), 4.06 (1H, d,15.2 Hz), 3.61 (2H, t, 6.3 Hz), 3.45-3.54 (2H, m), 3.22 (1H, br), 2.99(1H, ddd, 8.3, 2.6, 2.6 Hz), 2.36 (1H, ddd, 15.2, 3.6, 3.6 Hz),1.95-2.10 (3H, m), 1.58 (3H, d, 6.6 Hz).

EXAMPLE 18

Compound 18

Isomer ratio: about 10:1

FAB-MS m/z: 509 [M+H]⁺

Major component: ¹H-NMR (CDCl₃) δ(ppm): 10.76 (1H, br), 7.23 (1H, dd,15.5, 10.9 Hz), 6.84 (1H, br), 6.69 (1H, d, 16.2 Hz), 6.67 (1H, br),6.16 (1H, dd, 11.2, 10.6 Hz), 5.70 (1H, dd, 10.4, 3.1 Hz), 5.51 (1H, m),4.75 (1H, br), 4.64 (2H, s), 4.10 (1H, br), 3.45-3.57 (6H, m), 3.22 (1H,br), 2.99 (1H, ddd, 8.3, 2.6, 2.3 Hz), 2.36 (1H, ddd, 15.2, 3.6, 3.3Hz), 2.00 (1H, ddd, 15.2, 8.6, 4.0 Hz), 1.58 (3H, d, 6.6 Hz), 1.14 (3H,t, 7.1 Hz).

EXAMPLE 19

Compound 19

Isomer ratio: about 3:1

FAB-MS m/z: 477 [M+H]⁺

Major component: ¹H-NMR (CDCl₃) δ(ppm): 10.77 (1H, br), 7.47 (1H, br),7.24 (1H, dd, 16.1, 11.2 Hz), 6.68 (1H, d, 16.2 Hz), 6.61 (1H, s), 6.40(1H, br), 6.16 (1H, dd, 11.6, 11.5 Hz), 5.86 (1H, m), 5.70 (1H, dd,10.2, 3.3 Hz), 5.51 (1H, m), 5.23 (1H, dd, 17.2, 1.3 Hz), 5.16 (1H, dd,10.2, 1.3 Hz), 4.71 (1H, br), 4.64 (2H, s), 3.96-3.98 (3H, m), 3.21 (1H,br), 2.99 (1H, m), 2.35 (1H, ddd, 15.2, 3.6, 3.3 Hz), 1.98 (1H, ddd,15.2, 8.9, 4.0 Hz), 1.56 (3H, d, 6.9 Hz).

EXAMPLE 20

Compound 20

Isomer ratio: about 4:1

FAB-MS m/z: 533 [M+H]⁺

Major component: ¹H-NMR (CDCl₃) δ(ppm): 10.75 (1H, br), 8.17 (1H, br),7.24 (1H, dd, 16.2, 11.2 Hz), 6.68 (1H, d, 15.8 Hz), 6.42 (1H, t, 6.1Hz), 6.16 (1H, dd. 11.2, 10.6 Hz), 5.69 (1H, dd, 10.4, 3.1 Hz), 5.50(1H, m), 4.61 (2H, s), 4.04 (1H, d, 14.2 Hz), 3.09-3.27 (4H, m), 2.99(1H, m), 2.35 (1H, ddd, 15.2, 3.3, 3.3 Hz), 1.98 (1H, m), 1.68-1.73 (6H,br), 1.56 (3H, d, 6.6 Hz), 1.49 (1H, br), 1.10-1.24 (4H, br).

EXAMPLE 21

Compound 21

Isomer ratio: about 7:1

FAB-MS m/z: 617 [M+H]⁺

Major component: ¹H-NMR (CDCl₃) δ(ppm): 10.71 (1H, br), 7.75 (1H, br),7.20 (1H, dd, 16.0, 11.4 Hz), 6.64 (1H, d, 15.8 Hz), 6.54 (1H, s),6.52-6.64 (3H, m), 6.11 (1H, dd, 11.5, 10.2 Hz), 5.67 (1H, dd, 10.2, 3.3Hz), 5.46 (1H, m), 4.69 (1H, d, 13.5 Hz), 4.63 (1H, d, 16.2 Hz), 4.62(1H, br), 4.45 (1H, d, 5.9 Hz), 3.99 (1H, d, 15.8 Hz), 3.83 (3H, s),3.82 (3H, s), 3.81 (3H, s), 3.18 (1H, br), 2.96 (1H, m), 2.33 (1H, ddd,15.2, 3.6, 3.6 Hz), 1.95 (1H, ddd, 15.2, 8.6, 3.9 Hz), 1.52 (3H, d, 6.6Hz).

EXAMPLE 22

Compound 22

Isomer ratio: about 3:1

FAB-MS m/z: 528 [M+H]⁺

Major component: ¹H-NMR (CDCl₃) δ(ppm): 8.57 (1H, br s), 8.47 (1H, br d,4.3 Hz), 7.81 (1H, ddd, 8.2, 2.0, 1.7 Hz), 7.36 (1H, dd, 7.9, 4.6 Hz),7.20 (1H, dd, 15.8, 11.2 Hz), 6.93 (1H, t, 6.3 Hz), 6.65 (1H, d, 16.2Hz), 6.46 (1H, s), 6.10 (1H, dd, 10.6, 9.9 Hz), 5.67 (1H, dd, 10.2, 3.0Hz), 5.45 (1H, m), 4.48-4.64 (5H, m), 3.90 (1H, d, 15.2 Hz), 3.15 (1H,br), 2.94 (1H, br d, 8.9 Hz), 2.31 (1H, ddd, 15.2, 3.3, 3.3 Hz), 1.92(1H, m), 1.52 (3H, d, 6.9 Hz).

EXAMPLE 23

Compound 23

Isomer ratio: about 3:1

FAB-MS m/z: 544 [M+H]⁺

Major component: ¹H-NMR (CDCl₃) δ(ppm): 10.70 (1H, br), 9.02 (1H, br),7.22 (1H, dd, 15.8, 11.2 Hz), 6.61-6.65 (2H, m), 6.60 (1H, s), 6.53 (1H,m), 6.15 (1H, dd, 10.9, 10.6 Hz), 5.89-5.98 (2H, m), 5.68 (1H, dd, 10.2,3.0 Hz), 5.47 (1H, m), 4.64 (1H, d, 15.5 Hz), 4.61 (1H, br), 4.58 (1H,d, 16.2 Hz), 4.06 (1H, br), 3.41-3.06 (2H, m), 3.54 (3H, s), 3.23 (1H,br), 3.00 (1H, m), 2.81 (2H, m), 2.34 (1H, ddd, 15.2, 3.3, 3.3 Hz), 1.96(1H, ddd, 16.2, 8.9, 4.0 Hz), 1.55 (3H, d, 6.6 Hz).

EXAMPLE 24

Compounds 24 and 25

Compound 24

FAB-MS m/z: 548 [M+H]⁺

¹H-NMR (CDCl₃) δ(ppm): 7.61 (1H, br), 7.16 (1H, dd, 16.0, 11.4 Hz), 6.85(2H, br), 6.60 (1H, d, 16.2 Hz), 6.45 (1H, s), 5.79 (1H, dd, 11.2, 10.9Hz), 5.57 (1H, dd, 10.2, 3.0 Hz), 5.43 (1H, m), 4.70 (1H, br), 4.67 (1H,d, 15.8 Hz), 4.59 (1H, d, 15.8 Hz), 3.95 (1H, br), 3.51-3.72 (2H, m),3.15 (1H, br), 2.93 (1H, br d, 8.6 Hz), 2.80 (2H, t, 5.6 Hz), 2.72 (4H,br) 2.30 (1H, ddd, 14.9, 3.3, 3.3 Hz), 1.98 (1H, ddd, 14.9, 8.9, 4.0Hz), 1.52 (3H, d, 6.6 Hz), 1.45-1.63 (6H, br).

Compound 25

FAB-MS m/z: 548 [M+H]⁺

¹H-NMR (CDCl₃) δ(ppm): 8.58 (1H, br), 7.05 (1H, dd, 16.2, 11.2 Hz), 6.29(1H, s), 5.98 (1H, d, 16.2 Hz), 5.98 (1H, dd, 10.9, 9.2 Hz), 5.55 (1H,br d, 10.2 Hz), 5.45 (1H, m), 4.78 (1H, d, 15.8 Hz), 4.68 (1H, d, 15.5Hz), 4.07 (2H, br), 3.98 (1H, br), 3.69 (1H, br), 2.84-3.04 (8H, m),2.22 (1H, br d, 14.9 Hz), 2.04 (1H, ddd, 14.5, 10.4, 4.3 Hz), 1.54 (3H,d, 6.9 Hz), 1.20-1.48 (6H, br), 1.57 (3H, d, 6.9 Hz).

EXAMPLE 25

Compound 26

Isomer ratio: about 3:1

FAB-MS m/z: 562 [M+H]⁺

Major component: ¹H-NMR (CDCl₃) δ(ppm): 10.92 (1H, br), 9.00 (1H, br),7.17 (1H, m), 7.05 (1H, m), 6.81 (1H, d, 15.8 Hz), 6.56 (1H, s), 6.16(1H, t, 10.6 Hz), 5.63 (1H, dd, 10.4, 3.1 Hz), 5.44 (1H, m), 4.64 (1H,d, 19.5 Hz), 4.60 (1H, br), 4.57 (1H, d, 17.8 Hz), 4.06 (1H, br), 3.40(2H, t, 6.9 Hz), 3.25-3.36 (4H, m), 3.21 (1H, br), 2.96 (1H, br d, 8.2Hz), 2.30-2.42 (3H, m), 2.03 (2H, t, 7.6 Hz), 2.00 (1H, m), 1.77 (2H,m), 1.54 (3H, d, 6.6 Hz).

EXAMPLE 26

Compound 27

Isomer ratio: about 3:1

FAB-MS m/z: 505 [M+H]⁺

Major component: ¹H-NMR (CDCl₃) δ(ppm): 10.75 (1H, br), 8.50 (1H, br),7.23 (1H, dd, 16.0, 11.4 Hz), 6.67 (1H, d, 16.2 Hz), 6.61 (1H, s), 6.32(1H, d, 7.6 Hz), 6.14 (1H, dd, 11.9, 10.2 Hz), 5.68 (1H, dd, 10.4, 3.1Hz), 5.49 (1H, m), 4.67 (1H, d, 15.8 Hz), 4.58 (2H, s), 4.26 (1H, m),3.99 (1H, d, 15.8 Hz), 3.19 (1H, br), 2.96 (1H, m), 2.33 (1H, ddd 15.2,3.3, 3.3 Hz), 1.89-2.04 (3H, m), 1.58-1.66 (4H, m), 1.55 (3H, d, 6.6Hz), 1.38-1.43 (2H, m).

EXAMPLE 27

Compound 28

Isomer ratio: about 3:1

FAB-MS m/z: 513 [M+H]⁺

Major component: ¹H-NMR (CDCl₃) δ(ppm): 10.76 (1H, br), 7.48-7.56 (2H,m), 7.25-7.37 (3H, m), 7.07-7.16 (2H, m), 6.77 (1H, d, 16.2 Hz), 6.61(1H, s), 6.21 (1H, dd, 11.6, 10.6 Hz), 5.74 (1H, dd, 10.2, 3.6 Hz), 5.52(1H, m), 4.80 (1H, br), 4.73 (2H, s), 4.12 (1H, br), 3.23 (1H, br), 2.99(1H, ddd, 8.3, 3.3, 2.6 Hz), 2.36 (1H, ddd, 15.2, 3.6, 3.3 Hz), 1.99(1H, ddd, 15.2, 8.6, 4.0 Hz), 1.57 (3H, d, 6.9 Hz).

EXAMPLE 28

Compound 29

Isomer ratio: about 4:1

FAB-MS m/z: 555 [M+H]⁺

Major component: ¹H-NMR (CDCl₃) δ(ppm): 8.00 (1H, br s), 7.43 (2H, d,8.6 Hz), 7.19 (2H, d, 8.3 Hz), 7.20 (1H, m), 6.77 (1H, d, 16.2 Hz), 6.59(1H, s), 6.19 (1H, dd, 10.6, 9.9 Hz), 5.73 (1H, dd, 10.2, 3.3 Hz), 5.49(1H, m), 4.72 (2H, s), 4.72 (1H, br), 4.09 (1H, br), 3.22 (1H, br),2.82-3.01 (2H, m), 2.35 (1H, dd, 15.2, 3.3, 3.3 Hz), 1.98 (1H, ddd,15.2, 8.6, 4.0 Hz), 1.55 (3H, d, 6.6 Hz), 1.22 (6H, d, 6.9 Hz).

EXAMPLE 29

Compound 30

Isomer ratio: about 3:1

FAB-MS m/z: 543 [M+H]⁺

Major component: ¹H-NMR (CDCl₃) δ(ppm): 7.97 (1H, d 9.2 Hz), 7.38-7.44(2H, m), 7.26 (1H, dd, 15.8, 11.5 Hz), 6.81-6.86 (2H, m), 6.75 (1H, d,16.2 Hz), 6.56 (1H, s), 6.16 (1H, dd, 11.6, 10.2 Hz), 5.69 (1H, dd,10.6, 3.3 Hz), 5.47 (1H, m), 4.73 (1H, d, 16.5 Hz), 4.67 (1H, d, 14.9Hz), 4.64 (1H, br), 4.04 (1H, d, 14.5 Hz), 3.75 (3H, s), 3.20 (1H, br),2.96 (1H, ddd, 9.9, 3.6, 2.3 Hz), 2.33 (1H, ddd, 15.2, 3.6, 3.3 Hz),1.94 (1H, ddd, 15.2, 8.9, 4.0 Hz), 1.53 (3H, d, 6.9 Hz).

EXAMPLE 30

Compound 31

Isomer ratio: about 3:1

FAB-MS m/z: 584 [M+H]⁺

Major component: ¹H-NMR (CDCl₃) δ(ppm): 7.98 (1H, br s), 7.32 (2H, d,8.9 Hz), 7.29 (1H, m), 6.75 (1H, d, 16.2 Hz), 6.64 (2H, d, 8.9 Hz), 6.58(1H, s), 6.18 (1H, dd, 11.9, 9.9 Hz), 5.71 (1H, dd, 10.2, 3.0 Hz), 5.48(1H, m), 4.72 (1H, d, 16.8 Hz), 4.71 (2H, s), 4.04 (1H, d 15.8 Hz), 3.31(4H, q, 7.1 Hz), 3.21 (1H, br), 2.99 (1H, ddd, 8.6, 2.6, 2.3 Hz), 2.34(1H, ddd, 15.2, 3.6, 3.3 Hz), 1.96 (1H, ddd, 15.2, 8.6, 4.0 Hz), 1.55(3H, d, 6.6 Hz), 1.12 (6H, t, 7.1 Hz).

EXAMPLE 31

Compound 32

Isomer ratio: about 3:1

FAB-MS m/z: 514 [M+H]⁺

Major component: ¹H-NMR (CDCl₃) δ(ppm): 8.56 (1H, br d, 7.9 Hz), 8.46(1H, m), 8.30-8.34 (2H, m), 7.31-7.42 (2H, m), 6.76 (1H, d, 16.2 Hz),6.52 (1H, s), 6.17 (1H, dd, 10.9, 9.9 Hz), 5.72 (1H, dd, 10.2, 3.0 Hz),5.48 (1H, m), 4.80 (1H, br), 4.77 (1H, d, 16.5 Hz), 4.70 (1H, d, 16.5Hz), 4.03 (1H, d, 16.5 Hz), 3.20 (1H, br), 2.95 (1H, m), 2.34 (1H, ddd,15.2, 3.3, 3.3 Hz), 1.97 (1H, ddd, 15.2, 8.9, 4.0 Hz), 1.56 (3H, d, 6.9Hz).

EXAMPLE 32

Compound 33

Isomer ratio: about 3:1

FAB-MS m/z: 480 [M+H]⁺

Major component: ¹H-NMR (CDCl₃) δ(ppm): 10.77 (1H, br s), 7.24 (1H, dd,16.2, 11.2 Hz), 7.00 (1H, br s), 6.67 (1H, d, 16.5 Hz), 6.64 (1H, s),6.17 (1H, dd, 11.2, 10.6 Hz), 5.71 (1H, dd, 10.2, 3.0 Hz), 5.53 (1H, m),4.75 (1H, br), 4.62 (2H, s), 4.08 (1H, br), 3.22 (1H, br), 2.99 (1H, brd, 8.3 Hz), 2.63 (6H, s), 2.36 (1H, ddd, 14.8, 3.6, 3.6 Hz), 1.99 (1H,ddd, 15.5, 8.6, 4.1 Hz, 1.57 (3H, d, 6.6 Hz).

EXAMPLE 33

Compound 34

Isomer ratio: about 3:1

FAB-MS m/z: 496 [M+H]⁺

Major component: ¹H-NMR (CDCl₃) δ(ppm): 10.70 (1H, br), 7.72 (1H, br),7.24 (1H, dd, 15.2, 11.5 Hz), 6.66 (1H, d, 16.2 Hz), 6.60 (1H, s), 6.17(1H, dd, 11.9, 10.2 Hz), 5.72 (1H, dd, 10.4, 3.5 Hz), 5.51 (1H, m), 4.70(1H, br), 4.70 (2H, s), 4.10 (1H, br), 3.62 (2H, t, 4.6 Hz), 2.96-2.98(3H, m), 2.36 (1H, ddd, 15.5, 3.8, 3.3 Hz), 2.00 (1H, ddd, 15.5, 8.6,4.0 Hz), 1.58 (3H, d, 6.9 Hz).

EXAMPLE 34

Compound 35

Isomer ratio: about 3:1

FAB-MS m/z: 528 [M+H]⁺

Major component: ¹H-NMR (CDCl₃) δ(ppm): 10.75 (1H, br), 8.01 (1H, br s),7.19-7.25 (2H, m), 7.00 (1H, dd, 15.2, 10.9 Hz), 6.86-6.93 (4H, m), 6.71(1H, d, 16.2 Hz), 6.58 (1H, s), 6.18 (1H, dd, 10.6, 9.9 Hz), 5.72 (1H,dd, 10.4, 3.1 Hz), 5.50 (1H, m), 4.82 (1H, br), 4.76 (2H, s), 4.12 (1H,d, 14.2 Hz), 3.22 (1H, br), 2.97 (1H, m), 2.35 (1H, ddd, 15.2, 3.6, 3.3Hz), 1.99 (1H, ddd, 15.2, 8.6, 4.3 Hz), 1.55 (3H, d, 6.6 Hz).

EXAMPLE 35

Compound 36

Isomer ratio: about 4:1

FAB-MS m/z: 529 [M+H]⁺

Major component: ¹H-NMR (CDCl₃) δ(ppm): 8.30 (1H, br), 8.10 (1H, br d,4.6 Hz), 8.07 (1H, br), 7.52 (1H, dd, 7.6, 6.6 Hz), 7.22 (1H, m),6.67-6.87 (3H, m), 6.54 (1H, s), 6.15 (1H, dd, 11.2, 10.9 H), 5.70 (1H,dd, 10.2, 3.0 Hz), 5.48 (1H, m), 4.74 (2H, s), 4.67 (1H, d, 15.5 Hz),4.08 (1H, br), 3.23 (1H, br), 2.98 (1H, br d, 8.3 Hz), 2.35 (1H, br d,15.5 Hz), 1.98 (1H, m), 1.55 (3H, d, 6.6 Hz).

EXAMPLE 36

Compound 37

Isomer ratio: about 2:1

FAB-MS m/z: 520 [M+H]⁺

Major component: ¹H-NMR (CDCl₃) δ(ppm): 10.80 (1H, br), 8.50 (1H, br),7.25 (1H, dd, 15.8, 11.2 Hz), 7.06 (1H, s), 6.67 (1H, d, 13.5 Hz), 6.64(1H, s), 6.16 (1H, dd, 11.2, 10.9 Hz), 5.70 (1H, dd, 10.2, 3.0 Hz), 5.50(1H, m), 4.69 (1H, d, 15.8 Hz), 4.62 (2H, s), 4.01 (1H, d, 14.9 Hz),3.19 (1H, br), 2.96 (1H, m), 2.73 (4H, br), 2.34 (1H, ddd, 15.2, 3.6,3.0 Hz), 1.96 (1H, ddd, 15.2, 8.4, 4.1 Hz), 1.66 (6H, br), 1.56 (3H, d,6.9 Hz).

EXAMPLE 37

Compound 38

Isomer ratio: about 2:1

FAB-MS m/z: 535 [M+H]⁺

Major component: ¹H-NMR (CDCl₃) δ(ppm): 7.25 (1H, m), 7.14 (1H, s), 6.68(1H, 16.2 Hz), 6.44 (1H, s), 6.16 (1H, dd, 11.2, 10.9 Hz), 5.72 (1H, dd,10.1, 2.8 Hz), 5.49 (1H, m), 4.74 (1H, br), 4.64 (1H, 16.5 Hz), 4.57(1H, 16.5 Hz), 4.01 (1H, br), 3.20 (1H, br), 2.93-2.99 (5H, br), 2.76(4H, br), 2.45 (1H, m), 2.37 (6H, s), 1.97 (1H, m), 1.56 (3H, d, 6.6Hz).

EXAMPLE 38

Compound 39

According to (1-1) described in Example 1, an oxime derivative wasprepared from radicicol and trifluoroacetate of compound a, and thencompound 39 was prepared according to (1-2) described in Example 1.

Isomer ratio: about 5:1

FAB-MS m/z: 589 [M+H]⁺

Major component: ¹H-NMR (CDCl₃+CD₃OD) δ(ppm): 10.85 (1H, br), 7.90 (1H,br), 7.16 (1H, m), 6.67 (1H, d, 15.8 Hz), 6.58 (1H, s), 6.15 (1H, dd,11.6, 10.6 Hz), 5.64 (1H, br d, 9.9 Hz), 5.50 (1H, m), 4.75 (1H, br),4.19 (2H, m), 4.02 (1H, br), 3.55 (2H, br), 3.40 (2H, br), 3.19 (1H,br), 2.97 (1H, ddd, 7.9, 2.4, 2.4 Hz), 2.29-2.36 (3H, m), 1.99 (1H, ddd,15.2, 8.9, 4.0 Hz), 1.59-1.64 (10H, br), 1.56 (3H, d, 6.6 Hz), 1.37 (6H,br).

EXAMPLE 39

Compound 40

According to Example 38, compound 40 was prepared from atrifluoroacetate of compound b.

Isomer ratio: about 2:1

FAB-MS m/z: 631 [M+H]⁺

Major component: ¹H-NMR (CDCl₃) δ(ppm): 11.03 (1H, br), 8.72 (1H, br),7.16 (1H, dd, 15.8, 12.9 Hz), 6.67 (1H, d, 16.2 Hz), 6.58 (1H, s), 6.14(1H, dd, 11.2, 9.9 Hz), 5.62 (1H, br d, 9.6 Hz), 5.49 (1H, m), 4.72 (1H,br), 4.05-4.21 (3H, m), 3.56 (2H, br), 3.40 (2H, br), 3.21 (1H, br),2.97 (1H, ddd, 8.3, 2.3, 2.3 Hz), 2.29-2.37 (3H, m), 2.01 (1H, ddd,15.2, 8.6, 4.3 Hz), 1.60-1.76 (10H, br), 1.55 (3H, d, 6.6 Hz), 1.28(12H, br).

EXAMPLE 40

Compound 41

According to (1-2) described in Example 1, 14 mg (yield, 10%) ofcompound 41 was prepared from 100 mg (0.228 mmol) of compound (K), 52 mg(0.342 mmol) of HOBt, 65 mg (0.342 mmol) of EDCI and 69 mg (0.274 mmol)of pentaethylene glycol monomethyl ether. The thus prepared compound 41was found to be a mixture of oxime-based isomers (about 3:1) accordingto ¹H-NMR.

FAB-MS m/z: 672 [M+H]⁺

Major component: ¹H-NMR (CDCl₃) δ(ppm): 7.20 (1H, m), 6.77 (1H, d, 16.2Hz), 6.58 (1H, s), 6.16 (1H, dd, 11.6, 10.6 Hz), 5.66 (1H, br d, 9.6Hz), 5.53 (1H, m), 4.77 (1H, br), 4.76 (1H, d, 16.5 Hz), 4.69 (1H, 16.2Hz), 4.33 (2H, m), 4.00 (1H, br), 3.72 (2H, m), 3.64-3.65 (14H, m),3.53-3.56 (2H, m), 3.37 (3H, s), 3.20 (1H, br), 2.98 (1H, br d, 8.6 Hz),2.34 (1H, ddd, 15.2, 3.6, 3.3 Hz), 2.00 (1H, ddd, 15.5, 8.6, 4.0 Hz),1.56 (3H, d, 6.6 Hz).

EXAMPLE 41

Compound 42

According to Example 40, compound 42 was prepared from compound (K).

Isomer ratio: about 3:1

FAB-MS m/z: 584 [M+H]⁺

Major component: ¹H-NMR (CDCl₃) δ(ppm): 10.80 (1H, br), 7.20 (1H, m),6.77 (1H, d, 16.2 Hz), 6.58 (1H, br), 6.58 (1H, s), 6.16 (1H, t, 10.9Hz), 5.67 (1H, br d, 9.9 Hz), 5.51 (1H, m), 4.78 (1H, br), 4.76 (1H, d,16.5 Hz), 4.69 (1H, d, 16.5 Hz), 4.31-4.35 (2H, m), 4.02 (1H, br), 3.73(2H, t, 4.8 Hz), 3.63-3.67 (6H, m), 3.54-3.57 (2H, m), 3.38 (3H, s),3.19 (1H, br), 2.98 (1H, ddd, 9.2, 3.3, 3.3 Hz), 2.34 (1H, ddd, 15.2,3.6, 3.3 Hz), 1.98 (1H, ddd, 18.8, 8.9, 4.0 Hz), 1.57 (3H, d, 6.9 Hz).

EXAMPLE 42

Compound 43

According to (1-1) described in Example 1, 338 mg (yield, 53%) ofcompound 43 was prepared from 500 mg (1.37 mmol) of radicicol and 438 mg(2.74 mmol) of o-benzylhydroxylamine hydrochloride. The thus preparedcompound 43 was found to be a mixture of oxime-based isomers (about 2:1)according to ¹H-NMR.

FAB-MS m/z: 470 [M+H]⁺

Major component: ¹H-NMR (CD₃OD) δ(ppm): 7.10-7.50 (6H, m), 6.78 (1H, d,15.8 Hz), 6.42 (1H, s), 6.18 (1H, t, 10.9 Hz), 5.59 (1H, dd, 10.9, 3.3Hz), 5.30 (1H, m), 5.16 (2H, s), 3.91 (1H, d, 16.3 Hz), 3.81 (1H, d,16.3 Hz), 3.32 (1H, m), 3.01 (1H, dt, 7.9, 3.3 Hz), 2.41 (1H, dd, 14.3,3.5 Hz), 1.55 (1H, m), 1.52 (3H, d, 6.4 Hz).

EXAMPLE 43

Compound 44

A 205 mg (1.12 mmol) portion of compound c was dissolved in 3 ml ofmethanol, and the solution was mixed with 0.467 ml of 12N hydrochloricacid and stirred at room temperature for 2.5 hours. The solvent wasevaporated under reduced pressure, the thus prepared residue wasdissolved in 2 ml of pyridine and mixed with 136 mg (0.37 mmol) ofradicicol which had been dissolved in 2 ml of pyridine, and then themixture was stirred at room temperature for 138 hours. The reactionsolution was mixed with 0.5N hydrochloric acid and extracted with ethylacetate. The ethyl acetate layer was washed with saturated brine anddried with anhydrous sodium sulfate, and then the solvent was evaporatedunder reduced pressure. The resulting residue was purified by thin layerchromatography (chloroform/methanol=5/1, then chloroform/acetone=4/1) toobtain 119 mg (yield, 65%) of compound 44. The thus prepared compound 44was found to be a mixture of oxime-based isomers (about 2.5:1) accordingto ¹H-NMR.

FAB-MS m/z: 486 [M+H]⁺

Major component: ¹H-NMR (CDCl₃) δ(ppm): 11.00 (1H, br), 9.09 (1H, br),7.22-7.32 (3H, m), 7.00 (1H, d, 8.2 Hz), 6.91 (1H, ddd, 7.6, 7.3, 1.1Hz), 6.64 (1H, d, 15.8 Hz), 6.57 (1H, s), 6.14 (1H, dd, 9.9, 9.6 Hz),5.69 (1H, br d, 10.2 Hz), 5.47 (1H, m), 5.15 (1H, d, 13.5 Hz), 5.08 (1H,d, 12.9 Hz), 4.80 (1H, br), 3.99 (1H, br), 3.20 (1H, br), 2.96 (1H, ddd,8.3, 2.6, 2.5 Hz), 2.31 (1H, ddd, 15.2, 3.6, 3.3 Hz), 1.97 (1H, ddd,14.9, 8.6, 4.0 Hz), 1.55 (3H, d, 6.6 Hz).

EXAMPLES 44-49

According to Example 43, compounds 45 to 50 were prepared from radicicoland compounds d to i, respectively.

EXAMPLE 44

Compound 45

Isomer ratio: about 1.7:1

FAB-MS m/z: 502 [M+H]⁺

Major component: ¹H-NMR (CDCl₃+CD₃OD) δ(ppm): 7.11 (1H, dd, 16.2, 11.2Hz), 6.67 (1H, d, 16.2 Hz), 6.37 (1H, s), 6.35 (1H, d, 2.0 Hz), 6.32(1H, d, 2.0 Hz), 6.18 (1H, d, 2.0 Hz), 6.05 (1H, t, 10.6 Hz), 5.54 (1H,dd, 10.1, 2.8 Hz), 5.36 (1H, m), 4.97 (2H, s), 4.36 (1H, d, 16.2 Hz),3.86 (1H, d, 18.1 Hz), 3.16 (1H, br), 2.91 (1H, br d, 8.9 Hz), 2.26 (1H,ddd, 14.9, 3.3, 3.0 Hz), 1.77 (1H, ddd, 14.9, 4.3, 4.0 Hz), 1.47 (3H, d,6.6 Hz).

EXAMPLE 45

Compound 46

Isomer ratio: about 1.8:1

FAB-MS m/z: 560 [M+H]⁺

Major component: ¹H-NMR (CDCl₃) δ(ppm); 7.17 (1H, dd, 15.8, 11.5 Hz),6.73 (1H, d, 16.2 Hz), 6.63 (2H, s), 6.54 (1H, s), 6.13 (1H, dd, 12.5,10.6 Hz), 5.60 (1H, br d, 11.2 Hz), 5.49 (1H, m), 5.11 (2H, s), 4.69(1H, br), 4.04 (1H, br), 3.85 (3H, s), 3.84 (6H, s), 3.18 (1H, br), 2.96(1H, br d, 8.9 Hz), 2.32 (1H, ddd, 14.9, 3.6, 3.3 Hz), 1.95 (1H, ddd,14.5, 9.4, 4.1 Hz), 1.54 (3H, d, 6.6 Hz).

EXAMPLE 46

Compound 47

Isomer ratio: about 1.8:1

FAB-MS m/z: 500 [M+H]⁺

Major component: ¹H-NMR (CDCl₃) δ(ppm): 7.16 (1H, dd, 16.5, 11.2 Hz),6.74 (1H, d, 16.2 Hz), 6.52 (1H, s), 6.21 (1H, d, 2.0 Hz), 6.18 (1H, d,2.0 Hz), 6.14 (1H, dd, 10.9, 10.6 Hz), 5.98 (1H, dd, 3.6, 2.0 Hz), 5.65(1H, br d, 10.2 Hz), 5.49 (1H, m), 5.02 (1H, s), 4.70 (1H, br), 3.99(1H, br), 3.18 (1H, br), 2.96 (1H, ddd, 8.9, 3.3, 2.6 Hz), 2.32 (1H,ddd, 15.2, 3.6, 3.3 Hz), 1.96 (1H, ddd, 15.0, 9.4, 4.5 Hz), 1.55 (3H, d,6.9 Hz).

EXAMPLE 47

Compound 48

Isomer ratio: about 3:1

FAB-MS m/z: 527 [M+H]⁺

Major component: ¹H-NMR (CDCl₃) δ(ppm); 7.15 (1H, m), 7.14 (2H, d, 8.6Hz), 6.72 (2H, d, 8.6 Hz), 6.69 (1H, d, 15.8 Hz), 6.56 (1H, s), 6.14(1H, dd, 11.2, 10.6 Hz), 5.64 (1H, dd, 10.2, 3.3 Hz), 5.50 (1H, m), 4.73(1H, br), 4.25-4.38 (2H, m), 4.06 (1H, br), 3.21 (1H, br), 2.95-3.00(3H, m), 2.92 (6H, s), 2.34 (1H, ddd, 15.2, 3.5, 3.3 Hz), 1.99 (1H, ddd,14.8, 8.9, 4.0 Hz), 1.57 (3H, d, 6.9 Hz).

EXAMPLE 48

Compound 49

Isomer ratio: about 2.4:1

FAB-MS m/z: 582 [M+H]⁺

Major component: ¹H-NMR (CDCl₃) δ(ppm): 7.38 (2H, d, 7.9 Hz), 7.14-7.32(1H, m), 7.23 (2H, d, 7.6 Hz), 6.71 (1H, d, 15.8 Hz), 6.38 (1H, s), 6.15(1H, dd, 11.9, 10.6 Hz), 5.64 (1H, dd, 10.2, 2.0 Hz), 5.47 (1H, m), 5.17(2H, s), 4.70 (1H, br), 3.68 (1H, br), 3.66 (2H, s), 3.21 (1H, br), 2.97(1H, br d, 8.3 Hz), 2.61 (8H, br), 2.37 (3H, s), 2.33 (1H, ddd, 14.2,3.6, 3.3 Hz), 1.99 (1H, m), 1.54 (3H, d, 6.6 Hz).

EXAMPLE 49

Compound 50

Isomer ratio: about 1.4:1

FAB-MS m/z: 577 [M+H]⁺

Major component: ¹H-NMR (CDCl₃) δ(ppm): 7.88 (1H, d, 7.9 Hz), 7.71 (1H,m), 7.57 (1H, dd, 7.9, 7.3 Hz), 7.42 (1H, d, 8.3, 7.3 Hz), 7.19 (1H, m),6.79 (1H, d, 16.2 Hz), 6.56 (1H, s), 6.17 (1H, dd, 10.9, 9.6 Hz),5.59-5.72 (3H, m), 5.51 (1H, m), 4.66 (1H, br), 3.96 (1H, br), 3.20 (1H,br), 2.99 (1H, ddd, 8.6, 2.6, 2.6 Hz), 2.80 (6H, s), 2.34 (1H, ddd,15.2, 3.6, 3.3 Hz), 1.97 (1H, m), 1.56 (3H, d, 6.6 Hz).

EXAMPLE 50

Compound 51

A 565 mg (4.55 mmol) portion of compound j was dissolved in 10 ml ofpyridine, and the solution was mixed with 0.4 ml of concentratedhydrochloric acid and 664 mg (1.82 mmol) of radicicol and stirred atroom temperature for 21 hours. The reaction solution was mixed with asaturated ammonium chloride aqueous solution and extracted with ethylacetate, the ethyl acetate layer was washed with saturated brine anddried with anhydrous sodium sulfate, and then the solvent was evaporatedunder reduced pressure. The resulting residue was purified by silica gelcolumn chromatography (chloroform/methanol=40/1) to obtain 694 mg(yield, 81%) of compound 51.

Isomer ratio: about 2:1

FAB-MS m/z: 471 [M+H]⁺

Major component: ¹H-NMR (CD₃OD) δ(ppm): 8.48 (1H, d, 4.0 Hz), 7.84 (1H,dt, 7.6, 1.8 Hz), 7.53 (1H, m), 7.33 (1H, m), 7.26 (1H, dd, 16.2, 11.2Hz), 6.87 (1H, d, 15.8 Hz), 6.40 (1H, s), 6.17 (1H, t, 10.9 Hz), 5.60(1H, dd, 10.9, 3.0 Hz), 5.28 (1H, m), 5.23 (2H, s), 3.92 (1H, d, 16.2Hz), 3.77 (1H, d, 16.2 Hz), 3.33 (1H, m), 3.01 (1H, m), 2.40 (1H, ddd,14.2, 3.6, 3.3 Hz), 1.58 (1H, ddd, 13.8, 8.9, 4.4 Hz), 1.51 (3H, d, 6.3Hz).

EXAMPLE 51

Compounds 52 and 53

A mixture of compounds 52 and 53 (about 4:1) was prepared from radicicoland compound k according to Example 50, 380 mg of the thus preparedmixture of compounds 52 and 53 (about 4:1) was separated by highperformance liquid chromatography (column: YMC-Pack ODS AM, SH-365-10AM,500×30 mm I.D., eluent; 50 mM phosphate buffer (pH 7.3)/methanol=47/53,flow rate: 40 ml/min, detection: UV 276 nm), the eluate was extractedwith ethyl acetate, washed with saturated brine and dried with anhydroussodium sulfate, and then the solvent was evaporated under reducedpressure. Each of the resulting residues was powdered from a mixedsolvent of ethanol and water to obtain 219 mg of compound 52 and 133 mgof compound 53.

Compound 52

FAB-MS m/z: 471 [M+H]⁺

¹H-NMR (CD₃OD) δ(ppm): 8.58 (1H, d, 2.0 Hz), 8.47 (1H, dd, 5.0, 2.0 Hz),7.89 (1H, dd, 7.9, 2.0 Hz), 7.43 (1H, ddd, 7.9, 5.0, 2.0 Hz), 7.26 (1H,dd, 15.8, 10.9 Hz), 6.76 (1H, d, 15.8 Hz), 6.41 (1H, s), 6.16 (1H, t,10.9 Hz), 5.61 (1H, dd, 10.9, 3.0 Hz), 5.31 (1H, m), 5.22 (2H, s), 3.91(1H, d, 15.8 Hz), 3.81 (1H, d, 16.3 Hz), 3.35 (1H, m), 3.02 (1H, m),2.42 (1H, dt, 15.3, 4.0 Hz), 1.58 (1H, ddd, 13.8, 8.9, 4.4 Hz), 1.52(3H, d, 6.4 Hz).

Compound 53

FAB-MS m/z: 471 [M+H]⁺

¹H-NMR (CD₃OD) δ(ppm): 8.61 (1H, d, 2.0 Hz), 8.49 (1H, dd, 5.0, 2.0 Hz),7.93 (1H, dd, 7.9, 2.0 Hz), 7.45 (1H, ddd, 7.9, 5.0, 2.0 Hz), 7.15 (1H,dd, 16.2, 10.9 Hz), 6.41 (1H, s), 6.12 (1H, d, 15.8 Hz), 6.09 (1H, t,10.9 Hz), 5.48 (1H, dd, 10.9, 3.0 Hz), 5.31 (1H, m), 5.26 (2H, s), 4.64(1H, d, 16.4 Hz), 3.40 (1H, d, 16.2 Hz), 3.35 (1H, m), 2.96 (1H, dt,8.9, 2.6 Hz), 2.42 (1H, dt, 14.5, 3.0 Hz), 1.60 (1H, m), 1.50 (3H, d,6.40 Hz).

EXAMPLE 52

Compound 54

According to Example 50, compound 54 was prepared from radicicol andcompound m.

Isomer ratio: about 2:1

FAB-MS m/z: 471 [M+H]⁺

Major component: ¹H-NMR (CD₃OD) δ(ppm): 8.60 (2H, m), 7.50 (1H, m), 7.29(1H, dd, 16.2, 11.2 Hz), 6.85 (1H, d, 11.2 Hz), 6.43 (1H, s), 6.18 (1H,t, 10.9 Hz), 5.62 (1H, dd, 10.6, 3.3 Hz), 5.30 (1H, m), 5.23 (2H, s),3.91 (1H, d, 16.2 Hz), 3.81 (1H, d, 16.2 Hz), 3.35 (1H, m), 3.02 (1H,dt, 7.9, 3.3 Hz), 2.42 (1H, dd, 14.5, 4.0 Hz), 1.59 (1H, ddd, 13.8, 8.9,4.4 Hz), 1.52 (3H, d, 6.3 Hz).

EXAMPLE 53

Compound 55

According to Example 43, compound 55 was prepared from radicicol andcompound n.

Isomer ratio: about 1.5:1

FAB-MS m/z: 499 [M+H]⁺

Major component: ¹H-NMR (CDCl₃) δ(ppm): 8.47 (1H, s), 8.42 (1H, d, 5.0Hz), 7.62 (1H, d, 7.9 Hz), 7.28 (1H, dd, 7.6, 4.9 Hz), 7.17 (1H, dd,15.5, 11.5 Hz), 6.63 (1H, d, 16.2 Hz), 6.52 (1H, s), 6.15 (1H, dd, 11.6,11.2 Hz), 5.65 (1H, br d, 9.9 Hz), 5.50 (1H, m), 4.71 (1H, d, 15.5 Hz),4.20 (2H, t, 6.8 Hz), 4.01 (1H, br), 3.19 (1H, br), 2.97 (1H, br d, 8.6Hz), 2.77 (2H, t, 7.3 Hz), 2.33 (2H, ddd, 15.2, 3.3, 3.0 Hz), 2.07 (2H,m), 1.94 (1H, ddd, 16.8, 8.3, 4.0 Hz), 1.56 (3H, d, 6.9 Hz).

EXAMPLE 54

Compound 56

According to Example 43, compound 56 was prepared from radicicol andcompound o.

Isomer ratio: about 3:1

FAB-MS m/z: 487 [M+H]⁺

Major component: ¹H-NMR (CDCl₃) δ(ppm): 10.95 (1H, br), 9.36 (1H, br),8.15 (1H, d, 4.3 Hz), 7.34 (1H, d, 8.3 Hz), 7.20-7.30 (2H, m), 6.69 (1H,d, 16.2 Hz), 6.57 (1H, s), 6.15 (1H, dd, 10.9, 10.6 Hz), 5.70 (1H, br d,11.2 Hz), 5.48 (1H, m), 5.32 (1H, d, 12.5 Hz), 5.24 (1H, d, 12.5 Hz),4.77 (1H, br), 4.03 (1H, br), 3.19 (1H, br), 2.96 (1H, br d, 8.2 Hz),2.32 (1H, ddd, 15.2, 3.3, 3.0 Hz), 1.97 (1H, ddd, 14.7, 8.7, 4.3 Hz),1.55 (3H, d, 6.6 Hz).

EXAMPLE 55

Compound 57

(55-1):

A 5.00 g (13.7 mmol) portion of radicicol was dissolved in 10 ml of DMFto which, while cooling in an ice bath, were subsequently added 2.80 g(41.1 mmol) of imidazole and 4.54 g (30.1 mmol) oftert-butyl(chloro)dimethylsilane, and the resulting mixture was stirredat room temperature for 3 hours. The reaction solution was mixed with asaturated ammonium chloride aqueous solution and extracted with ethylacetate, the ethyl acetate layer was washed with saturated brine anddried with anhydrous sodium sulfate, and then the solvent was evaporatedunder reduced pressure. The resulting residue was purified by silica gelcolumn chromatography (chloroform/methanol=100/1) to obtain 6.96 g(yield, 86%) of a di-tert-butyldimethylsilyl derivative of radicicol.

FAB-MS m/z: 593 [M+H]⁺

(55-2):

According to (1-1) described in Example 1, 18 mg (yield, 5.5%) ofcompound (L) was prepared from 319 mg (0.54 mmol) ofdi-tert-butyldimethylsilyl derivative of radicicol and 240 mg (3.45mmol) of hydroxylamine hydrochloride. The thus prepared compound (L) wasfound to be a mixture of oxime-based isomers (about 1:1) according to¹H-NMR.

FAB-MS m/z: 608 [M+N]⁺

(55-3):

A 120 mg (0.20 mmol) portion of compound (L) was dissolved in 1.7 ml ofTHF, the resulting solution was mixed with 167 mg (0.99 mmol) of2-hydroxymethyl-3-methoxymethoxypyridine dissolved in 0.5 ml of THF,which had been prepared by dimethoxymethylation of3-hydroxy-2-pyridinecarboxylic acid and subsequent reduction withlithium aluminum hydride, 103 mg (0.39 mmol) of triphenylphosphine and0.06 ml (0.39 mmol) of DEAD, and the mixture was stirred at roomtemperature for 23 hours. The reaction solution was mixed with aphosphate buffer (pH 7) and extracted with ethyl acetate. The ethylacetate layer was washed with saturated brine and dried with anhydroussodium sulfate, and then the solvent was evaporated under reducedpressure. The resulting residue was purified by thin layerchromatography (chloroform/methanol=100/1) to obtain 39 mg (yield, 26%)of a di-tert-butyldimethylsilyl derivative of compound 57.

FAB-MS m/z: 761 [M+H]⁺

(55-4):

A 39 mg (0.05 mmol) portion of the di-tert-butyldimethylsilyl derivativeof compound 57 was dissolved in 1.8 ml of THF, 0.13 ml (0.13 mmol) of a1M TBAF/THF solution was added to the thus prepared solution which wascooled at −10° C., and the resulting mixture was stirred for 50 minutesat the same temperature. The reaction solution was mixed with aphosphate buffer (pH 7) and extracted with chloroform. The chloroformlayer was washed with saturated brine and dried with anhydrous sodiumsulfate, and then the solvent was evaporated under reduced pressure. Theresulting residue was purified by thin layer chromatography(chloroform/methanol=12/1) to obtain 26 mg (yield, 95%) of compound 57.The thus prepared compound 57 was found to be a mixture of oxime-basedisomers (about 1:1.7) according to ¹H-NMR.

FAB-MS m/z: 531 [M+H]⁺

Major component: ¹H-NMR (CDCl₃) δ(ppm): 11.15 (1H, br), 8.28 (1H, dd,4.6, 1.3 Hz), 7.49 (1H, d, 8.3 Hz), 7.25 (1H, dd, 8.3, 5.0 Hz), 7.02(1H, dd, 16.2, 10.9 Hz), 6.72 (1H, s), 6.13 (1H, d, 15.8 Hz), 6.09 (1H,dd, 10.2, 9.6 Hz), 5.55 (1H, dd, 10.6, 2.3 Hz), 5.49 (1H, m), 5.30 (2H,s), 5.23 (2H, s), 4.58 (1H, d, 16.5 Hz), 4.21 (1H, d, 16.5 Hz), 3.45(3H, s), 3.08 (1H, br), 2.90 (1H, br d, 9.9 Hz), 2.31 (1H, ddd, 15.2,3.0, 2.6 Hz), 1.90 (1H, ddd, 15.2, 10.2, 4.3 Hz), 1.53 (3H, d, 6.9 Hz).

EXAMPLE 56

Compound 58

According to Example 43, compound 58 was prepared from radicicol andcompound p.

Isomer ratio: about 1.4:1

FAB-MS m/z: 487 [M+H]⁺

Major component: ¹H-NMR (CDCl₃+CD₃OD) δ(ppm): 8.15 (0.25H, dd, 5.9, 3.3Hz), 7.76 (0.25H, dd, 5.9, 3.3 Hz), 7.64 (1H, m), 7.33 (1H, dd, 3.3, 2.6Hz), 7.11 (1H, dd, 16.0, 11.4 Hz), 6.56 (1H, d, 16.2 Hz), 6.50 (0.5H, d,1.7 Hz), 6.38 (1H, s), 6.05 (1H, dd, 10.9, 9.6 Hz), 5.56 (1H, dd, 10.2,3.0 Hz), 5.37 (1H, m), 4.86 (2H, s), 4.46 (1H, d, 1.65 Hz), 3.88 (1H, d,16.5 Hz), 3.18 (1H, br), 2.90 (1H, ddd, 8.6, 2.6, 2.3 Hz), 2.27 (1H,ddd, 14.9, 4.3, 3.6 Hz), 1.79 (1H, ddd, 14.5, 8.9, 4.0 Hz), 1.47 (3H, d,6.3 Hz).

EXAMPLE 57

Compound 59

According to (1-1) described in Example 1, compound 59 was prepared fromradicicol and a trifluoroacetate of compound q.

Isomer ratio: about 2:1

FAB-MS m/z: 504 [M+H]⁺

Major component: ¹H-NMR (CD₃OD) δ(ppm): 7.29 (1H, dd, 15.8, 11.2 Hz),6.82 (1H, d, 16.2 Hz), 6.43 (1H, s), 6.18 (1H, dd, 15.8, 10.9 Hz), 5.67(1H, s), 5.66 (1H, dd, 10.6, 3.6 Hz), 5.31 (1H, m), 4.87 (2H, s), 3.95(1H, d, 16.2 Hz), 3.84 (1H, d, 16.2 Hz), 3.30 (1H, m), 3.02 (1H, dd,5.6, 2.3 Hz), 2.43 (1H, dt, 14.3, 3.5 Hz), 1.62 (1H, m), 1.52 (3H, d,6.6 Hz).

EXAMPLE 58

Compound 60

According to Example 43, compound 60 was prepared from radicicol andcompound r.

Isomer ratio: about 2:1

FAB-MS m/z: 491 [M+H]⁺

Major component: ¹H-NMR (CDCl₃) δ(ppm): 8.88 (2H, br), 7.19 (1H, m),6.66 (1H, d, 12.9 Hz), 6.38 (1H, s), 6.16 (1H, dd, 12.1, 9.9 Hz), 5.62(1H, br d, 10.2 Hz), 5.42 (1H, m), 4.59 (1H, br), 3.86-4.00 (3H, m),3.11-3.31 (3H, m), 2.95 (1H, br d, 8.3 Hz), 2.53 (3H, s), 2.11-2.33 (3H,m), 1.95 (1H, m), 1.78 (4H, br), 1.53 (3H, d, 6.6 Hz).

EXAMPLE 59

Compound 61

According to (1-1) described in Example 1, compound 61 was prepared fromradicicol and a hydrochloride of compound s.

Isomer ratio: about 1.8:1

FAB-MS m/z: 477 [M+H]⁺

Major component: ¹H-NMR (CD₃OD) δ(ppm): 7.27 (1H, dd, 16.5, 11.6 Hz),6.75 (1H, d, 16.5 Hz), 6.39 (1H, s), 6.15 (1H, dd, 11.6, 10.6 Hz), 5.61(1H, dd, 10.6, 3.6 H), 5.32 (1H, m), 4.38 (2H, m), 3.95 (2H, m), 3.28(1H, m), 3.20 (2H, m), 3.03 (4H, m), 2.95 (1H, m), 2.41 (1H, m), 1.95(4H, m), 1.66 (1H, m), 1.52 (3H, d, 6.3 Hz).

EXAMPLE 60

Compound 62

According to (1-1) described in Example 1, compound 62 was prepared fromradicicol and a hydrochloride of compound t.

Isomer ratio: about 5:1

FAB-MS m/z: 505 [M+H]⁺

Major component: ¹H-NMR (CD₃OD) δ(ppm): 7.26 (1H, dd, 15.8, 10.9 Hz),6.72 (1H, d, 16.2 Hz), 6.42 (1H, s), 6.16 (1H, dd, 11.9, 10.6 Hz), 5.62(1H, dd, 10.6, 3.6 Hz), 5.30 (1H, m), 4.23 (2H, dd, 12.5, 6.3 Hz), 3.96(1H, d, 16.2 Hz), 3.81 (1H, d, 16.2 Hz), 3.35 (1H, m), 3.15 (6H, m),3.03 (1H, m), 2.44 (1H, dt, 14.5, 3.6 Hz), 2.15 (2H, m), 1.80-1.86 (4H,m), 1.66 (1H, m), 1.52 (3H, d, 6.3 Hz).

EXAMPLE 61

Compound 63

According to (1-1) described in Example 1, compound 63 was prepared fromradicicol and a hydrochloride of compound u.

Isomer ratio: about 2:1

FAB-MS m/z: 521 [M+H]⁺

Major component: ¹H-NMR (CD₃OD) δ(ppm): 7.25 (1H, dd, 16.2, 11.9 Hz),6.72 (1H, d, 16.2 Hz), 6.44 (1H, s), 6.16 (1H, dd, 11.9, 10.6 Hz), 5.61(1H, dd, 10.6, 3.6 Hz), 5.31 (1H, m), 4.24 (2H, m), 3.96 (1H, d, 16.2Hz), 3.89 (1H, m), 3.83 (1H, d, 16.2 Hz), 3.43 (1H, m), 3.35 (1H, m),2.96-3.10 (5H, m), 2.43 (1H, dt, 10.9, 3.6 Hz), 1.95-2.20 (4H, m),1.75-1.80 (4H, m), 1.62 (1H, m), 1.52 (3H, d, 6.6 Hz).

EXAMPLE 62

Compound 64

According to (1-1) described in Example 1, compound 64 was prepared fromradicicol and a hydrochloride of compound v.

Isomer ratio: about 3:1

FAB-MS m/z: 521 [M+H]⁺

Major component: ¹H-NMR (CD₃OD) δ(ppm): 7.24 (1H, dd, 16.2, 11.9 Hz),6.73 (1H, d, 16.2 Hz), 6.42 (1H, s), 6.15 (1H, m), 5.60 (1H, dd, 10.8,4.0 Hz), 5.30 (1H, m), 4.17 (2H, m), 3.92 (1H, d, 16.2 Hz), 3.80 (1H, d,16.2 Hz), 3.70 (2H, m), 3.35 (1H, m), 3.27 (4H, m), 3.02 (1H, ddd, 8.9,3.3, 2.0 Hz), 2.41-2.56 (7H, m), 1.70 (5H, m), 1.53 (3H, d, 6.6 Hz).

EXAMPLE 63

Compound 65

According to (1-1) described in Example 1, compound 65 was prepared fromradicicol and a hydrochloride of compound w.

Isomer ratio: about 4:1

FAB-MS m/z: 520 [M+H]⁺

Major component: ¹H-NMR (CD₃OD) δ(ppm): 7.24 (1H, dd, 16.2, 11.2 Hz),6.71 (1H, d, 16.2 Hz), 6.42 (1H, s), 6.15 (1H, dd, 10.9, 9.6 Hz), 5.60(1H, dd, 10.9, 3.3 Hz), 5.31 (1H, m), 4.18 (2H, dt, 4.3, 2.0 Hz), 3.93(1H, d, 15.8 Hz), 3.83 (1H, d, 15.8 Hz), 3.35 (1H, m), 3.02 (1H, dd,8.9, 2.3 Hz), 2.45-2.60 (10H, m), 2.45 (1H, dt, 14.5, 3.6 Hz), 2.36 (3H,s), 1.92 (2H, m), 1.62 (1H, m), 1.53 (3H, d, 6.6 Hz).

EXAMPLE 64

Compound 66

According to (1-1) described in Example 1, compound 66 was prepared fromradicicol and a hydrochloride of compound x.

Isomer ratio: about 1.5:1

FAB-MS m/z: 596 [M+H]⁺

Major component: ¹H-NMR (CD₃OD) δ(ppm): 7.20-7.30 (3H, m), 6.95 (2H, d,7.9 Hz), 6.84 (1H, t, 7.4 Hz), 6.74 (1H, d, 16.2 Hz), 6.43 (1H, s), 6.11(1H, m), 5.59 (1H, dd, 10.6, 3.3 Hz), 5.30 (1H, m), 4.20 (2H, m), 3.95(1H, d, 15.8 Hz), 3.84 (1H, d, 15.8 Hz), 3.34 (1H, m), 3.19 (4H, m),3.01 (1H, dd, 5.6, 3.3 Hz), 2.71 (4H, m), 2.52 (2H, m), 2.40 (1H, dd,14.5, 3.6 Hz), 1.74 (4H, m), 1.61 (1H, m), 1.51 (3H, d, 6.6 Hz).

EXAMPLE 65

Compound 67

According to (1-1) described in Example 1, compound 67 was prepared fromradicicol and a hydrochloride of compound y.

Isomer ratio: about 2:1

FAB-MS m/z: 537 [M+H]⁺

Major component: ¹H-NMR (CD₃OD) δ(ppm): 7.24 (1H, dd, 16.2, 11.2 Hz),6.73 (1H, d, 16.2 Hz), 6.42 (1H, s), 6.15 (1H, dd, 10.9, 9.6 Hz), 5.59(1H, dd, 10.9, 3.3 Hz), 5.30 (1H, m), 4.11-4.19 (2H, m), 3.94 (1H, d,16.2 Hz), 3.84 (1H, d, 16.2 Hz), 3.34 (1H, m), 3.00 (1H, m), 2.78 (4H,m), 2.67 (4H, m), 2.47 (3H, m), 1.67 (5H, m), 1.53 (3H, d, 6.6 Hz).

EXAMPLE 66

Compounds 68 and 69

According to (1-1) described in Example 1, a mixture of compounds 68 and69 was prepared from radicicol and a hydrochloride of compound z, andthen compounds 68 and 69 were prepared by purifying the mixture usinghigh performance liquid chromatography (eluent: 50 mM phosphate buffer(pH 5.9)/acetonitrile=68/32) according to Example 51.

Compound 68: FAB-MS m/z: 491 [M+H]⁺

¹H-NMR (CDCl₃) δ(ppm): 10.08 (1H, br s), 7.18 (1H, dd, 15.5, 11.5 Hz),6.85 (1H, br s), 6.63 (1H, d, 15.5 Hz), 6.60 (1H, s), 6.15 (1H, t, 11.5Hz), 5.67 (1H, d, 11.5 Hz), 5.51 (1H, m), 4.73 (1H, br), 4.29 (2H, t,5.3 Hz), 4.03 (1H, br), 3.64 (2H, m), 3.51 (3H, m), 3.20 (1H, s), 2.98(1H, m), 2.40 (2H, m), 2.33 (1H, m), 2.01 (2H, m), 1.57 (3H, d, 6.9 Hz).

Compound 69: FAB-MS m/z: 491 [M+H]⁺

¹H-NMR (CDCl₃) δ(ppm): 11.25 (1H, br s), 7.02 (1H, dd, 16.0, 11.2 Hz),6.58 (1H, br s), 6.11 (1H, d, 16.0 Hz), 6.09 (1H, m), 5.57 (1H, d, 10.9Hz), 5.51 (1H, m), 4.45 (1H, d, 16.5 Hz), 4.34 (2H, d, 5.2 Hz), 4.25(1H, d, 16.5 Hz), 3.80 (1H, m), 3.58 (3H, m), 3.08 (1H, s), 2.91 (1H, d,9.9 Hz), 2.45 (2H, m), 2.32 (1H, m), 2.06 (2H, m), 1.95 (1H, m), 1.56(3H, d, 6.9 Hz).

EXAMPLE 67

Compound 70

According to Example 50, compound 70 was prepared from radicicol andcompound aa.

Isomer ratio: about 2:1

FAB-MS m/z: 505 [M+H]⁺

Major component: ¹H-NMR (CD₃OD) δ(ppm): 7.25 (1H, dd, 16.2, 11.8 Hz),6.75 (1H, d, 16.2 Hz), 6.43 (1H, s), 6.17 (1H, t, 11.2 Hz), 5.60 (1H,dd, 10.6, 3.6 Hz), 5.30 (1H, m), 4.18 (2H, m), 3.92 (1H, d, 16.2 Hz),3.79 (1H, d, 16.2 Hz), 3.49 (2H, m), 3.41 (2H, q, 6.9 Hz), 3.34 (1H, m),3.02 (1H, m), 2.43 (1H, m), 2.37 (2H, m), 2.04 (2H, m), 1.98 (2H, m),1.62 (1H, m), 1.53 (3H, d, 6.6 Hz).

EXAMPLE 68

Compound 71

According to (1-1) described in Example 1, compound 71 was prepared fromradicicol and a trifluoracetate of compound bb.

Isomer ratio: about 3:1

FAB-MS m/z: 507 [M+H]⁺

Major component: ¹H-NMR (CD₃OD) δ(ppm): 7.24 (1H, dd, 16.5, 11.2 Hz),6.77 (1H, d, 16.2 Hz), 6.45 (1H, s), 6.17 (1H, dd, 10.9, 9.6 Hz), 5.61(1H, m), 5.29 (1H, m), 4.11-4.90 (3H, m), 3.99 (1H, d, 16.2 Hz), 3.81(1H, d, 16.2 Hz), 3.39 (4H, m), 3.31 (1H, m), 3.01 (1H, m), 2.43 (1H,dt, 14.5, 3.6 Hz), 2.07 (4H, m), 1.60 (1H, m), 1.51 (3H, d, 6.6 Hz).

EXAMPLE 69

Compound 72

According to Example 50 compound 72 was prepared from radicicol andcompound cc.

Isomer ratio: about 2:1

FAB-MS m/z: 580 [M+H]⁺

Major component: ¹H-NMR (CD₃OD) δ(ppm): 7.24 (1H, dd, 16.2, 11.2 Hz),6.72 (1H, d, 16.2 Hz), 6.43 (1H, s), 6.11 (1H, dd, 11.9, 10.6 Hz), 5.59(1H, dd, 10.6, 3.3 Hz), 5.31 (1H, m), 4.99 (1H, t, 5.0 Hz), 3.81-3.99(6H, m), 3.35 (1H, m), 2.99 (1H, m), 2.42 (1H, dt, 14.5, 3.5 Hz), 2.03(2H, m), 1.61 (1H, ddd, 14.2, 4.6, 4.6 Hz), 1.53 (3H, d, 6.3 Hz).

EXAMPLE 70

Compound 73

(70-1):

A 300 mg (0.493 mmol) portion of compound (L) was dissolved in 5 ml ofdichloromethane to which were subsequently added 0.05 ml (0.493 mmol) ofethyl chloroformate and 0.07 ml (0.493 mmol) of triethylamine at −78°C., and the mixture was stirred at 0° C. for 2 hours. The reactionsolution was mixed with a saturated ammonium chloride aqueous solutionand extracted with ethyl acetate. The ethyl acetate layer was washedwith saturated brine and dried with anhydrous sodium sulfate, and thenthe solvent was evaporated under reduced pressure. The resulting residuewas purified by silica gel column chromatography (n-hexane/ethylacetate=6/1) to obtain 188 mg (yield, 56%) of adi-tert-butyldimethylsilyl derivative of compound 73.

(70-2):

According to (55-4) described in Example 55, compound 73 was preparedfrom the di-tert-butyldimethylsilyl derivative of compound 73.

Isomer ratio: about 1.3:1

Major component: ¹H-NMR (CD₃OD) δ(ppm): 7.45 (1H, dd, 16.3, 11.4 Hz),6.71 (1H, d, 15.8 Hz), 6.46 (1H, s), 6.22 (1H, m), 5.73 (1H, dd, 10.4,3.0 Hz), 5.33 (1H, m), 4.34 (1H, d, 6.9 Hz), 4.11 (1H, d, 16.3 Hz), 4.00(1H, d, 16.3 Hz), 3.35 (1H, m), 3.04 (1H, m), 2.43 (1H, dt, 14.3, 3.5Hz), 1.61 (1H, m), 1.53 (3H, d, 6.4 Hz), 1.35 (3H, t, 6.9 Hz).

EXAMPLE 71

Compound 74

According to (70-1) and (70-2) described in Example 70, compound 74 wasprepared from compound (L), triethylamine and methyl isocyanate.

Isomer ratio: about 1.2:1

Major component: ¹H-NMR (CD₃OD) δ(ppm): 7.42 (1H, dd, 16.3, 11.9 Hz),6.76 (1H, d, 16.3 Hz), 6.46 (1H, s), 6.26 (1H, dd, 11.9, 10.6 Hz), 5.71(1H, dd, 10.9, 3.5 Hz), 5.34 (1H, m), 4.10 (1H, d, 16.3 Hz), 3.85 (1H,d, 16.3 Hz), 3.36 (1H, m), 3.04 (1H, m), 2.85 (3H, s), 2.43 (1H, dt,14.3, 3.5 Hz), 1.65 (1H, m), 1.53 (3H, d, 6.4 Hz).

EXAMPLE 72

Compound 75

According to (70-1) and (70-2) described in Example 70, compound 75 wasprepared from compound (L), triethylamine and acetyl chloride.

Isomer ratio: about 1.2:1

Major component: ¹H-NMR (CD₃OD) δ(ppm): 7.43 (1H, dd, 15.8, 11.9 Hz),6.75 (1H, d, 15.8 Hz), 6.47 (1H, s), 6.15 (1H, dd, 11.9, 10.6 Hz), 5.72(1H, dd, 10.4, 3.5 Hz), 5.34 (1H, m), 4.13 (1H, d, 16.3 Hz), 4.04 (1H,d, 16.3 Hz), 3.35 (1H, m), 3.04 (1H, m), 2.40 (1H, dt, 14.3, 3.5 Hz),2.23 (3H, s), 1.65 (1H, m), 1.53 (3H, d, 6.9 Hz).

EXAMPLE 73

Compound 76

According to (1-1) described in Example 1, compound 76 was prepared fromradicicol and O-phenylhydroxylamine hydrochloride.

Isomer ratio: about 3:1

FAB-MS m/z: 456 [M+H]⁺

Major component: ¹H-NMR (CDCl₃) δ(ppm): 10.95 (1H, br), 7.24-7.38 (5H,m), 7.05 (1H, m), 6.89 (1H, d, 16.2 Hz), 6.61 (1H, s), 6.23 (1H, ddd,10.2, 10.2, 1.1 Hz), 5.73 (1H, br d, 10.2 Hz), 5.53 (1H, m), 4.85 (1H,br), 4.21 (1H, br), 3.23 (1H, br), 3.01 (1H, ddd, 8.3, 2.6, 2.3 Hz),2.37 (1H, ddd, 15.2 3.6, 3.3 Hz), 2.01 (1H, ddd, 15.5, 9.1, 3.8 Hz),1.58 (3H, d, 6.6 Hz).

REFERENCE EXAMPLE 1

Compound a

(1-1)

A 5.00 g (22.4 mmol) portion of 8-bromooctanoic acid was dissolved in amixed solvent of 2 ml dichloromethane and 10 ml hexane, and the solutionwas mixed with 8.00 ml (44.8 mmol) of tert-butyl2,2,2-trichloroacetoimidate and 0.45 ml (3.66 mmol) of borontrifluoride-ether complex and stirred at room temperature for 1 hour.The reaction solution was mixed with 10 ml of hexane and 0.031 g (3.66mmol) of sodium bicarbonate, the resulting precipitate was separated byfiltration, and then the solvent was evaporated under reduced pressure.The resulting residue was purified by silica gel column chromatography(n-hexane/ethyl acetate=5/1) to obtain 2.34 g (yield, 38%) of tert-butyl8-bromooctanoate.

(1-2)

A 2.70 g (8.29 mmol) portion of tert-butyl 8-bromooctanoate wasdissolved in 20 ml of DMF, and the solution was mixed with 1.35 g (8.28mmol) N-hydroxyphthalimide and 1.86 ml (12.4 mmol) of1,8-diazabicyclo[5,4,0]-7-undecene and stirred at room temperature for20.5 hours. The reaction solution was mixed with water and extractedwith ethyl acetate, the ethyl acetate layer was washed with 0.5Nhydrochloric acid and then with saturated brine and dried with anhydroussodium sulfate, subsequently evaporating the solvent under reducedpressure. The resulting residue was purified by silica gel columnchromatography (n-hexane/ethyl acetate=5/1) to obtain 0.83 g (yield,28%) of tert-butyl 8-(phthalimidoxy)-octanoate.

¹H-NMR (CDCl₃) δ(ppm): 7.83 (2H, m), 7.75 (2H, m), 4.20 (2H, t, 6.8 Hz),2.21 (2H, t, 7.6 Hz), 1.79 (2H, m), 1.60 (2H, m), 1.44 (9H, s),1.45-1.29 (6H, m).

(1-3)

A 1.00 g (2.77 mmol) portion of tert-butyl 8-(phthalimidoxy)-octanoatewas dissolved in 9 ml of chloroform, and the solution was mixed with 4.1ml (4.16 mmol) of a 1M hydrazine monohydrate/methanol solution andstirred at room temperature for 0.5 hour. After separation of theresulting precipitate by filtration, the resulting filtrate was mixedwith water and extracted with chloroform, the chloroform layer waswashed with saturated brine and dried with anhydrous sodium sulfate, andthen the solvent was evaporated under reduced pressure. The thusprepared residue was dissolved in 14 ml of dichloromethane, and thesolution was mixed with 6.4 ml of trifluoroacetic acid and stirred atroom temperature for 2 hours. By evaporating the solvent under reducedpressure, a trifluoroacetate of the compound a was prepared.

REFERENCE EXAMPLE 2

Compound b

According to (1-1) to (1-3) described in Reference Example 1, atrifluoroacetate of compound b was prepared from 11-bromoundecanoicacid.

REFERENCE EXAMPLE 3

Compound c

(3-1)

According to (1-2) described in Reference Example 1, 1.29 g(quantitative) of methyl 2-methoxymethoxybenzoate was prepared from 1.00g (6.57 mmol) of methyl salicylate, 0.75 ml (9.86 mmol) of chloromethylmethyl ether and 1.72 ml (9.86 mmol) of diisopropylethylamine.

(3-2)

A 792 mg (4.04 mmol) portion of methyl 2-methoxymethoxybenzoatedissolved in 12 ml of THF was added to 337 mg (8.89 mmol) of lithiumaluminum hydride dissolved in 5 ml of THF, and the mixture was stirredat room temperature for 2.5 hours. The reaction solution was mixed withwater and extracted with ethyl acetate, and the ethyl acetate layer waswashed with saturated brine and dried with anhydrous sodium sulfate. Byevaporation of the solvent under reduced pressure, 640 mg (yield, 94%)of 2-methoxymethoxybenzyl alcohol was prepared.

(3-3)

According to (55-3) described in Example 55, 486 mg (yield, 57%) ofN-(2-methoxymethoxybenzyloxy)phthalimide was prepared from 454 mg (2.70mmol) of 2-methoxymethoxybenzyl alcohol, 484 mg (2.97 mmol) ofN-hydroxyphthalimide, 744 mg (2.84 mmol) of triphenylphosphine and 0.446ml (2.84 mmol) of DEAD.

(3-4)

According to (1-3) described in Reference Example 1, a reaction solutionprepared by treating 427 mg (1.36 mmol) ofN-(2-methoxymethoxybenzyloxy)phthalimide with 0.099 ml (2.04 mmol) ofhydrazine monohydrate was separated by filtration, and then the solventwas evaporated under reduced pressure to obtain 244 mg (yield, 98%) ofcompound c.

FAB-MS m/z: 184 [M+H]⁺

¹H-NMR (CDCl₃) δ(ppm): 7.37 (1H, dd, 7.4, 1.8 Hz), 7.27 (1H, ddd, 7.4,7.3, 1.8 Hz), 7.11 (1H, dd, 7.3, 1.3 Hz), 7.02 (1H, ddd, 7.6, 7.6, 1.3Hz), 5.42 (2H, br s), 5.22 (2H, s), 4.79 (2H, s), 3.49 (3H, s).

REFERENCE EXAMPLE 4

Compound d

According to (55-1) described in Example 55, methyl3,5-di-(tert-butyldimethylsiloxy)benzoate was prepared from methyl3,5-dihydroxybenzoate, and compound d was prepared from methyl3,5-di-(tert-butyldimethylsiloxy)benzoate according to (3-2) to (3-4)described in Reference Example 3.

FAB-MS m/z: 384 [M+H]⁺

¹H-NMR (CDCl₃) δ(ppm): 6.46 (2H, d, 2.3 Hz), 6.28 (1H, t, 2.3 Hz), 5.37(2H, br), 4.57 (2H, s), 0.97 (18H, s), 0.19 (12H, s).

REFERENCE EXAMPLE 5

Compound e

According to (3-2) to (3-4) described in Reference Example 3, compound ewas prepared from methyl 3,4,5-trimethoxybenzoate.

FAB-MS m/z: 214 [M+H]⁺

¹H-NMR (CDCl₃) δ(ppm): 6.60 (2H, s), 5.43 (2H, br), 4.64 (2H, s), 3.88(6H, s), 3.85 (3H, s).

REFERENCE EXAMPLE 6

Compound f

(6-1)

A 2.00 g (13.1 mmol) portion of 3,5-diaminobenzoic acid was dissolved ina mixed solvent of 20 ml THF and 20 ml water, and the solution was mixedwith 6.88 g (31.5 mmol) of di-tert-butyl dicarbonate, adjusted to pH 7to 8 with a saturated sodium bicarbonate aqueous solution and thenstirred at room temperature for 4 hours. The reaction solution was mixedwith a 10% citric acid aqueous solution and extracted with ethylacetate. The ethyl acetate layer was washed with saturated brine anddried with anhydrous sodium sulfate, and then the solvent was evaporatedunder reduced pressure. The resulting residue was purified by silica gelcolumm chromatography (chloroform/methanol=10/1) to obtain 3.93 g(yield, 85%) of 3,5-di-(tert-butoxycarbonylamino)benzoic acid.

(6-2)

A 2.00 g (5.68 mmol) portion of 3,5-di-(tert-butoxycarbonylamino)benzoicacid was dissolved in 15 ml of THF, 3.77 ml (39.7 mmol) of borane-methylsulfide complex dissolved in 10 ml of THF was added dropwise to the thusprepared solution, and the mixture was stirred at room temperature for 5hours. The reaction solution was cooled to 0° C., mixed with water andextracted with ethyl acetate. The ethyl acetate layer was washed withsaturated brine and dried with anhydrous sodium sulfate, and then thesolvent was evaporated under reduced pressure. The resulting residue waspurified by silica gel column chromatography (chloroform/methanol=20/1)to obtain 1.08 g (yield, 56%) of1,3-di-tert-butoxycarbonylamino-5-hydroxymethylbenzene.

(6-3)

According to (3-3) and (3-4) described in Reference Example 3, compoundf was prepared from1,3-di-tert-butoxycarbonylamino-5-hydroxymethylbenzene.

FAB-MS m/z: 354 [M+H]⁺

¹H-NMR (CDCl₃) δ(ppm): 7.41 (1H, t, 1.7 Hz), 7.07 (2H, d, 1.7 Hz), 6.50(2H, br s), 5.39 (2H, br), 4.62 (2H, s), 1.50 (18H, s).

REFERENCE EXAMPLE 7

Compound g

According to (3-3) and (3-4) described in Reference Example 3, compoundg was prepared from 4-(dimethylamino)phenetyl alcohol.

FAB-MS m/z: 181 [M+H]⁺

¹H-NMR (CDCl₃) δ(ppm): 7.10 (2H, d, 8.6 Hz), 6.70 (2H, d, 8.6 Hz), 5.38(2H, br s), 3.84 (2H, t, 7.1 Hz), 2.91 (6H, s), 2.81 (2H, t, 7.1 Hz).

REFERENCE EXAMPLE 8

Compound h

According to (6-2) and (6-3) described in Reference Example 6, compoundh was prepared from 4-(N-methylpiperazinomethyl)benzoic acid.

¹H-NMR (CDCl₃) δ(ppm): 7.29 (2H, m), 7.15 (2H, m), 5.20 (2H, br), 4.56(2H, s), 3.93 (2H, s), 3.44-3.41 (4H, br), 2.68-2.58 (4H, m), 2.55 (3H,s).

REFERENCE EXAMPLE 9

Compound i

According to (1-2) described in Reference Example 1, methyl2-(dimethylaminosulfonyl)benzoate was prepared from methyl2-(aminosulfonyl)benzoate, methyl iodide and potassium carbonate, andthen compound i was prepared according to (3-2) to (3-4) described inReference Example 3.

FAB-MS m/z: 231 [M+H]⁺

¹H-NMR (CDCl₃+CD₃OD) δ(ppm): 7.87 (1H, d, 7.9 Hz), 7.71 (1H, d, 7.6 Hz),7.62 (1H, dd, 7.9, 7.3 Hz), 7.46 (1H, dd, 7.6, 7.3 Hz), 5.10 (2H, s),2.81 (6H, s).

REFERENCE EXAMPLE 10

Compound j

According to (3-3) and (3-4) described in Reference Example 3, compoundj was prepared from 2-pyridylcarbinol.

¹H-NMR (CDCl₃) δ(ppm): 7.21-7.30 (5H, m), 5.40 (2H, br), 3.90 (2H, t,6.9 Hz), 2.91 (2H, t, 6.9 Hz).

REFERENCE EXAMPLE 11

Compound k

According to (3-3) and (3-4) described in Reference Example 3, compoundk was prepared from 3-pyridylcarbinol.

¹H-NMR (CDCl₃) δ(ppm): 8.63 (1H, d, 2.0 Hz), 8.57 (1H, dd, 5.0, 1.5 Hz),7.73 (1H, dt, 7.9, 2.0 Hz), 7.33 (1H, dd, 7.9, 4.9 Hz), 4.92 (2H , br),4.71 (2H, s).

REFERENCE EXAMPLE 12

Compound m

According to (3-3) and (3-4) described in Reference Example 3, compoundm was prepared from 4-pyridylcarbinol.

¹H-NMR (CDCl₃) δ(ppm): 8.59 (2H, d, 5.9 Hz), 7.26 (2H, d, 5.9 Hz), 5.55(2H, br), 4.71 (2H, s).

REFERENCE EXAMPLE 13

Compound n

According to (3-3) and (3-4) described in Reference Example 3, compoundn was prepared from 3-pyridinepropanol.

¹H-NMR (CDCl₃) δ(ppm): 8.45 (1H, br s), 8.43 (1H, dd, 4.9, 1.3 Hz), 7.50(1H, ddd, 7.6, 1.6 1.3 Hz), 7.20 (1H, dd, 7.6, 4.9 Hz), 5.36 (2H , br),3.67 (2H, t, 6.3 Hz), 2.67 (2H, t, 7.8 Hz), 1.90 (2H, m).

REFERENCE EXAMPLE 14

Compound o

According to (3-1) to (3-4) described in Reference Example 3, compound owas prepared from 3-hydroxypinolinic acid.

FAB-MS m/z: 185 [M+H]⁺

¹H-NMR (CDCl₃) δ(ppm): 8.27 (1H, dd, 4.6 1.3 Hz), 7.42 (1H, dd, 8.3, 1.3Hz), 7.18 (1H, dd, 8.3, 4.6 Hz), 5.75 (2H, br), 5.22 (2H, d, 0.7 Hz),4.92 (2H, s), 3.47 (3H, d, 1.0 Hz).

REFERENCE EXAMPLE 15

Compound p

According to (3-1) to (3-4) described in Reference Example 3, compound pwas prepared from 6-hydroxynicotinic acid.

¹H-NMR (CDCl₃+CD₃OD) δ(ppm): 7.98 (1H, d, 2.3 Hz), 7.52 (1H, dd, 8.6,2.3 Hz), 6.68 (1H, d, 8.2 Hz), 5.32 (2H , s), 4.46 (2H, s), 3.35 (3H,s).

REFERENCE EXAMPLE 16

Compound q

(16-1)

According to (1-2) described in Reference Example 1, tert-butylN-(6-uracilmethoxy)carbamate was prepared from tert-butylN-hydroxycarbamate, sodium hydride, and 6-(chloromethyl)uracil.

FAB-MS m/z: 258 [M+H]⁺

¹H-NMR (CDCl₃) δ(ppm): 10.34 (1H, br), 8.02 (1H, br), 5.54 (1H, s), 4.67(2H, s), 1.48 (9H, s).

(16-2)

A 385 mg (1.50 mmol) portion of tert-butyl N-(6-uracilmethoxy)carbamatewas dissolved in 0.5 ml of dichloromethane, and the solution was mixedwith 0.5 ml of trifluoroacetic acid and stirred at room temperature for1 hour. By evaporating the solvent under reduced pressure, atrifluoroacetate of compound q was prepared.

REFERENCE EXAMPLE 17

Compound r

According to (3-3) and (3-4) described in Reference Example 3, compoundr was prepared from 1-methyl-3-piperidinemethanol.

¹H-NMR (CDCl₃) δ(ppm): 5.47 (2H, br), 3.55 (1H, dd, 9.9, 5.6 Hz), 3.48(1H, dd, 9.9, 7.6 Hz), 2.92 (1H, br d, 10.9 Hz), 2.81 (1H, br d, 11.2Hz), 2.28 (3H, s), 2.03 (1H, m), 1.89-1.97 (2H , m), 1.59-1.71 (4H, m).

REFERENCE EXAMPLE 18

Compound s

According to (3-3) described in Reference Example 3,1-(2-phthalimidoxyethyl)pyrrolidine was prepared from pyrrolidineethanoland treated with a 4N hydrochloric acid/ethyl acetate solution to makeit into a hydrochloride, and then compound s was prepared from thehydrochloride according to (3-4) described in Reference Example 3. Bytreating compound s with a 4N hydrochloric acid/ethyl acetate solution,a hydrochloride of compound s was prepared.

FAB-MS m/z: 145 [M+H]⁺

REFERENCE EXAMPLE 19

Compound t

(19-1)

According to (1-2) described in Reference Example 1, 4.20 g (yield, 39%)of ethyl N-(3-bromopropoxy)acetoimidate was prepared from 5.00 g (48.5mmol) of ethyl acetohydroxamate, 1.90 g (48.5 mmol) of sodium hydrideand 7.4 ml (72.7 mmol) of 1,3-dibromopropane.

(19-2)

A 500 mg (2.23 mmol) portion of ethyl N-(3-bromopropoxy)acetoimidate wasdissolved in 6 ml of dichloromethane, and the solution was mixed with0.22 ml (2.23 mmol) of piperidine and 0.33 ml (2.23 mmol) of1,8-diazabicyclo[5.4,0]-7-undecene and stirred at room temperature for36 hours. The reaction solution was mixed with a saturated ammoniumchloride aqueous solution and extracted with chloroform. The chloroformlayer was washed with saturated brine and dried with anhydrous sodiumsulfate, and then the solvent was evaporated under reduced pressure. Theresulting residue was purified by silica gel chromatography(chloroform/methanol=10/1) to obtain 166 mg (yield, 32%) of ethylN-(3-piperinopropoxy)acetoimidate.

FAB-MS m/z: 229 [M+H]⁺

¹H-NMR (CDCl₃) δ(ppm): 4.00 (2H, q, 6.9 Hz), 3.93 (2H, t, 6.3 Hz), 2.53(6H, m), 1.93 (2H, m), 1.92 (3H, s), 1.70 (4H, m), 1.49 (2H, m), 1.27(3H, t, 6.9 Hz).

(19-3)

A 166 mg (0.71 mmol) portion of ethylN-(3-piperidinopropoxy)acetoimidate was dissolved in 0.5 ml of THF, andthe solution was mixed with 0.1 ml of concentrated hydrochloric acid andstirred at room temperature for 1 hour. By evaporating the solvent underreduced pressure, a hydrochloride of compound t was prepared.

REFERENCE EXAMPLE 20

Compound u

According to (19-2) and (19-3) described in Reference Example 19, ahydrochloride of compound u was prepared from ethylN-(3-bromopropoxy)acetoimidate.

REFERENCE EXAMPLE 21

Compound v

According to (19-1) described in Reference Example 19, ethylN-(4-bromobutoxy)acetoimidate was prepared from ethyl acetohydroxamate,sodium hydride and 1,4-dibromobutane, and then a hydrochloride ofcompound v was prepared according to (19-2) and (19-3) described inReference Example 19.

REFERENCE EXAMPLE 22

Compound w

According to (19-2) and (19-3) described in Reference Example 19, ahydrochloride of compound w was prepared from ethylN-(3-bromopropoxy)acetoimidate.

REFERENCE EXAMPLE 23

Compound x

According to (19-2) and (19-3) described in Reference Example 19, ahydrochloride of compound x was prepared from ethylN-(4-bromobutoxy)acetoimidate.

REFERENCE EXAMPLE 24

Compound y

According to (19-2) and (19-3) described in Reference Example 19, ahydrochloride of compound y was prepared from ethylN-(4-bromobutoxy)acetoimidate.

REFERENCE EXAMPLE 25

Compound z

According to (3-3) and (3-4) described in Reference Example 3, compoundz was prepared from 1-(2-hydroxyethyl)-2-pyrrolidinone, and thencompound z was treated with a 4N hydrochloric acid/ethyl acetatesolution to obtain a hydroxhloride of compound z.

FAB-MS m/z: 145 [M+H]⁺

REFERENCE EXAMPLE 26

Compound aa

According to (3-3) and (3-4) described in Reference Example 3, compoundas was prepared from 1-(3-hydroxypropyl)-2-pyrrolidinone.

¹H-NMR (CDCl₃) δ(ppm): 5.40 (2H, br), 3.68 (2H , t, 6.3 Hz), 3.39 (2H,dd, 11.5, 6.9 Hz), 3.37 (2H, m), 2.39 (2H, dd, 8.6, 7.6 Hz), 2.02 (2H,ddd, 6.9, 6.3, 1.0 Hz), 1.81 (2H, ddd, 11.5, 6.3, 1.0 Hz), 1.81 (2H, m).

REFERENCE EXAMPLE 27

Compound bb

(27-1)

According to (16-1) described in Reference Example 16, 659 mg (3.80mmol) of tert-butyl N-(allyloxy)carbamate prepared from tert-butylN-hydroxycarbamate, sodium hydride and allyl bromide was dissolved in 10ml of dichloromethane, and the thus prepared solution was mixed with 886mg (4.67 mmol) of m-chloroperbenzoic acid and stirred at roomtemperature for 24 hours. The reaction solution was filtered, mixed witha 1N sodium hydroxide aqueous solution and extracted with chloroform.The chloroform layer was washed with saturated brine and dried withanhydrous sodium sulfate, and then the solvent was evaporated underreduced pressure. The resulting residue was purified by silica gelcolumn chromatography (n-hexane/ethyl acetate=4/1) to obtain 447 mg(yield, 62%) of tert-butyl N-(2,3-epoxypropoxy)carbamate.

(27-2)

A 150 mg (0.79 mmol) portion of tert-butyl N-(2,3-epoxypropoxy)carbamatewas dissolved in 1 ml of methanol, and the solution was mixed with 0.08ml (0.95 mmol) of pyrrolidine and stirred at room temperature for 14hours. The reaction solution was mixed with a saturated ammoniumchloride aqueous solution and extracted with chloroform. The chloroformlayer was washed with saturated brine and dried with anhydrous sodiumsulfate, and then the solvent was evaporated under reduced pressure toobtain 181 mg (yield, 88%) of tert-butylN-(2-hydroxy-3-pyrrolidinylpropoxy)carbamate.

FAB-MS m/z: 261 [M+H]⁺

¹H-NMR (CDCl₃) δ(ppm): 4.02 (1H, m), 3.92 (1H, dd, 11.2, 3.3 Hz), 3.77(1H , dd, 11.2, 7.3 Hz), 2.68 (4H, m), 2.65 (1H, m), 2.50 (1H, m), 1.89(9H, s), 1.80 (4H, m).

(27-3)

According to (16-2) described in Reference Example 16, atrifluoroacetate of compound bb was prepared from tert-butylN-(2-hydroxy-3-pyrrolidinylpropoxy)carbamate.

REFERENCE EXAMPLE 28

Compound cc

According to (1-2) described in Reference Example 1,2-(2-phthalimidoxyethyl)-1,3-dioxolan was prepared from2-(2-bromoethyl)-1,3-dioxolan, N-hydroxyphthalimide and potassiumcarbonate, and then compound cc was prepared from2-(2-phthalimidoxyethyl)-1,3-dioxolan according to (3-4) described inReference Example 3.

¹H-NMR (CDCl₃) δ(ppm): 5.40 (2H, br), 4.97 (1H, t, 5.0 Hz), 3.80-4.00(6H, m), 1.98 (2H, dt, 6.3, 5.0 Hz).

TABLE 6 Reference Example H₂NO—R^(3e) Compound R^(3e) a (CH₂)₇CO₂H b(CH₂)₁₀CO₂H c

d

e

f

g

h

i

j

k

m

n

o

p

q

r

s

t

u

v

w

x

y

z

aa

bb

cc

INDUSTRIAL APPLICABILITY

According to the present invention, novel radicicol derivatives orpharmacologically acceptable salts thereof which show tyrosine kinaseinhibition activity and have antitumor or immunosuppression effects areprovided.

What is claimed is:
 1. A radicicol derivative represented by formula (I) or a pharmacologically acceptable salt thereof:

wherein R¹ and R² independently represent hydrogen, alkanoyl, alkenoyl, tert-butylidiphenylsilyl or tert-butyldimethylsilyl; R³ represents (A) Y—R⁵ wherein Y represents substituted or unsubstituted alkylene; and R⁵ represents (a) substituted or unsubstituted pyrrolidonyl, or (b) substituted or unsubstituted pyrrolidinyl, (B) COR¹³ wherein R¹³ represents hydrogen, substituted or unsubstituted lower alkyl, substituted or unsubstituted higher alkyl, substituted or unsubstituted aryl, substituted or unsubstituted lower alkoxy, or NR¹⁴R¹⁵ (wherein R¹⁴ and R¹⁵ independently represent hydrogen, substituted or unsubstituted lower alkyl, substituted or unsubstituted higher alkyl, substituted or unsubstituted aryl, or R¹⁴ and R¹⁵ are combined together with adjoining N to represent a substituted or unsubstituted heterocyclic group), or (C) substituted or unsubstituted aryl; X represents halogen; and R⁴ represents hydrogen, alkanoyl, alkenoyl, or —SO—Z (wherein Z is represented by formula (A):

wherein R^(1A) and R^(2A) have the same meaning as R¹ and R², respectively; X^(A) represents halogen; and W represents O or N—O—R^(3A) wherein R^(3A) has the same meaning as R³), or X and R⁴ are combined to represent a single bond.
 2. The compound according to claim 1 or a pharmacologically acceptable salt thereof, wherein X is halogen.
 3. The compound according to claim 1 or a pharmacologically acceptable salt thereof, wherein X and R⁴ are combined to represent a single bond.
 4. The compound according to claim 3 or a pharmacologically acceptable salt thereof, wherein R¹ and R² each is hydrogen.
 5. The compound according to claim 4 or a pharmacologically acceptable salt thereof, wherein R³ is Y—R⁵.
 6. The compound according to claim 5 or a pharmacologically acceptable salt thereof, wherein R⁵ is substituted or unsubstituted pyrrolidonyl, or substituted or unsubstituted pyrrolidinyl.
 7. The compound according to claim 5 or a pharmacologically acceptable salt thereof, wherein R⁵ is pyrrolidonyl.
 8. A therapeutic agent of diseases caused by tyrosine kinase, which comprises at least one of the compounds according to any one of claims 1 to 7 or a pharmacologically acceptable salt thereof. 